Catalog tui ep tiet trung anios - 3 m - wipak

HOSPITALSCLINICS

GUIDEThe Hygiene and

Disinfection

2015EDITION

Laboratoires ANIOS key figures» 3 production sites in France (20.000m² of eco-controlled factories)» 1 Research centre» 600 employees» 350 formulas, 4000 product references» 25 packaging lines» 12.000 bottles packaged each day» 16.000m² of fi nished product storage

Certifications» QSE» ISO 9001» ISO 14001» OHSAS 18001» COFRAC accreditation

A family business

1918 René COLLET takes over the business from his father.

1953 Odette COLLET, daughter-in-law of Fernand COLLET-DELVAL, takes over from her husband.

1968 Luce LETARTRE-COLLET, grand-daughter of the founder, takes over the management of the company. She builds the expansion of the business on a partnership with the Pasteur Institute of Lille.

1974 Thierry LETARTRE creates disinfection products range in the hospital sector.

1982 Bertrand LETARTRE becomes C.E.O. of the company.

1986 Launch of the Medical and Dental division.

1989 Launch of the 1st totally automated production site, known at the time as one of the most modern in Europe.

1994 Creation of the Hydenet department (communities).

2000 Creation of a new distribution center with over 6.000 m².

2006 Opening of a second production site in the North of France.

2010 Construction of the «LUCE LETARTRE» Research Centre.

2013 Expansion of the distribution center (16.000m²).

2014 Acquisition of Soluscope.

1898Fernand COLLET-DELVAL, great grand-father of Bertrand and Thierry LETARTRE, creates the Laboratoires ANIOS, specialized in manufacting disinfectant products for breweries in Lille, North of France.

New viruses and bacteria having emerged in the last 110 years, bacterial resistance became a major world health issue.

What has not changed is our battle: to help YOU in the fi ght against microbes.You, as members of the caring professions, are at the heart of our

endeavours.

Our primary objective is to be by your side in your daily battle against hospital infections, not only by providing high-performance cleaning and disinfectant

products, but also in the monitoring and management of specifi c issues, the training of your teams in hygiene techniques and even in the research and

development of new formulas.

This proximity that we establish everyday, thanks to a fi eld team close to you, is necessary in order to understand your concerns and provide solutions: to ensure overall management of cleaning, disinfection and antisepsis.

In this publication, you will fi nd our complete range of products and devices, combining effi ciency, simplicity, safety and respect, both for the user and the environment.

EDITORIALby Bertrand and Thierry Letartre

Our products at your service.

Since 2012 : Member of the Private Organizations for Patient Safety Program launched by W.H.O.

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1000 m² dedicated to Research and Development

Associated services A strong field support

The Research Centre is also at your disposal for solving specific problems:» Evaluating the antimicrobial efficiency on field strains and critical surfaces.» Analyzing product/material compatibility, corrosion studies.» Implementing product trace studies, before and after rinsing.» Verifying the compatibility of a specific material with our products.

» Designs specific equipment in order to optimize the performance of products while respecting local constraints. » Ensures the production of airborne disinfection equipment, washbasins, endoscopy

modules, etc.

The Equipment Department Equipment adapted to your needs

Our Luce Letartre Research Centre, one of the mostimportant in Europe, includes: » 40 technicians» 3 laboratories: Chemistry and Formulation, Microbiology (COFRACaccredited) and Analytical Chemistry.

Its missions:» To develop innovative new formulations.» To evaluate the products efficiency against micro-organisms.» To verify the products compatibility on hospital materials.

Our products at your service.

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Our added value

A consistant service proposition Our Research Centre at your disposal

» Associated services to solve your specifi c problems (corrosion studies, product/material compatibility studies, etc.).» All of our product effi ciency tests are accessible from the scientifi c fi les available on demand.» Regulatory monitoring (e.g.: REACH, BIOCIDE, CLP...).

A whole team at your service:

» A large network of partners representing more than 500 sales representatives specialized in hygiene and disinfection » 11 area managers » 10 commercial assistants » A scientifi c team dedicated to support you and to answer your questions

Laboratoires ANIOS around the world

» Presence in more than 80 countries, i.e. more than 100% growth in 5 years » 1 representative offi ce in Hong Kong » 4 subsidiaries : Turkey, Argentina, Brazil and Italy

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For several years now, Laboratoires ANIOS have been committed to a voluntary business approach involving the three core values of its management system, namely: Quality, Safety and the Environment (QSE).

In order to give a clearer picture of our commitments, we have developed the ANIOSAFE company charter which, by going beyond compulsory regulations, is proof of our determination to fi ght microbes whilst respecting Humans and the Environment.

At every step in the life of ANIOS products, the ANIOSAFE charter obliges us to take the protection of the environment, or ecodesign, into account when manufacturing our products. Likewise, the charter also covers measures to control impact on Humans.

Our social and environmental commitment : ANIOSAFE

PRODUCTIONAN ECOLOGICALLY MANAGED SITE WITH 3 CERTIFICATIONS (ISO 9001, ISO 14001, OHSAS 18001)

• Connecting each production site to water treatment and purifi cation plants.

• Optimizing the consumption of rinsing water.

• Treating wastewater by fi xing a pollution rate below national requirements.

• Ensuring storage in a secondary containment facility in case of product leakage or runoff.

PACKAGING

• Favouring recyclable packaging.

• Gradual elimination of aerosol containers in favour of other dispersion systems.• Creating single-material packaging for easier recycling.• Researching and developping new solutions for biodegradable packaging.

• Eliminating CMR substances.

• Substituting whenever possible allergenic substances and Volatile Organic Compounds (VOC).

• Use of vegetal substances of oleo-chemical origin (new generation of surfactants).

• Looking for new generations of active ingredients and additives.

RAW MATERIALS AND FORMULATION:

ECO-FORMULATION

TRANSPORT

• Giving priority to concentrated products to reduce their impact on transport.

• Selecting transport companies that meet the EURO 5 and EURO 6 standards.

• Using vehicles with low CO2 emissions.

USE OF PRODUCTS

• Providing complete scientifi c studies detailing all formulation properties.

• Suggesting users on-site training in good practice for product usage.

• Providing ongoing training for sales teams in products, as well as technical and scientifi c knowledge.

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Descriptions of products and materials, references, 3D environments... Find our full-range offer in interactive format on our websitewww.anios.com

Rinsing and Rejuvenation Rinsing and Rejuvenation

anios RenovateuR dMi » Removes organic deposits. » Renews the instruments shine.

indicationsRenovating cleaning product for medico-surgical instrumentation. Allows the removal of organic deposits. Usable in machines, ultra-sonic tanks or manual soaking.

coMpositionPotassium hydroxide, sodium hypochlorite and deflocculating and dispersing agents.

packaging - Ref.2 cans, 5L each ..................................................................1677.509 10L can ..............................................................................1677.602

instRuctions foR use

anios Rn » neutralises alkaline products. » also suitable for short cycles of

tank washing. » complexing effect of minerals.

indicationsNeutralization of alkaline residues coming from detergents and water during the washing cycle in automatic washers of medico-surgical instruments and medical devices.

coMpositionFormulat based on phosphoric acid.

packaging - Ref.2 cans, 5L each ..................................................................193.038 10L can ..............................................................................193.024


autoMatic diLution Between 0,1 and 0,5%

autoMatic diLution oR

anios LuB » eliminates rust pitting. » eliminates mineral deposits. » eliminates protein traces, iron oxide deposits and other

oxide stains.

indicationsLubrification by soaking of articulated instrumentation.

coMpositionNon ionic surfactants, lubricating agent, preservative agents.

packaging - Ref.3 dosing bottles, 1L each ...................................................883.137

anios Rda » for a brighter instrumentation, without

trace. » drying activator with lubricant effect. » can be used in any quality of water

(osmotic or softened). » Highly compatible with polysulfones and

poM. » specially designed to use in

combination with anios detergents.

indicationsRinsing product for medico-surgical instruments and medical devices in an automatic machine supplied with osmotic or non-osmotic water. Lubricant effect coupled with a neutralising effect on alkaline residues from detergents and water during the washing cycle. Drying activator.

coMpositionCombination of non-ionic and anionic surfactants in an acid medium.

packaging - Ref.2 cans, 5L each ..................................................................2372.038 10L can ..............................................................................2372.024 25L can ..............................................................................2372.018


autoMatic diLution Between 0,03 and 0,1%

anios R444 » eliminates rust pitting, protein traces, iron oxide

deposits and other oxide stains. » eliminates mineral deposits. » soaking method: integrated dosing system. » compatible with any quality of dilution water.

indicationsA specific renovation product for stainless steel instruments and medical devices. Removes protein traces, iron oxide deposits and other oxide stains.

coMpositionPhosphoric acid, non ionic surfactants.

packaging - Ref.3 dosing bottles, 1L each ...................................................191.137

usable in ultra-sonic bin


pRoduct to Be diLuted 0.5 to 5% i.e. 5 to 50ml for 1L


pRoduct to Be diLuted 2.5% i.e. 25ml for 1L

pRoduct to Be diLuted 0.4 to 1% i.e. 4 to 10ml for 1L

NEW

HOW TO AVOID THE APPEARANCE OF TRACES?

scale is the result of the precipitation of calcium and magnesium in hard water, encouraged by high temperature and pH.To avoid scale residues and traces, we recommend:

• an intermediate acid Rinsing (with anios Rn)An acid rinse neutralises alkaline residues, solubilises mineral ions contained in the water and on instruments, maintaining the instrumentation’s brilliance.

• a final Rinsing (with anios Rda)A rinsing drying activator, thanks to its sequestering and solubilising agents, encourages, during the drying step, the elimination of residual water and avoid the appearance of traces resulting frommineral and scale residues contained in final rinse water.

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MACHINES AND TUNNELSMACHINES AND TUNNELS

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Dangerous. Respect the precautions for use.Use with caution. Read the label and information regarding the product before each use.

Information relating to the CE marking of our products and materials is included in our technical data sheets (available on demand).Produits dangereux. Respectez les précautions d’emploi.Utilisez avec précaution. Avant toute utilisation, lisez l’étiquette et les informations concernant le produit.

anios RenovateuR dMi» Removes organic deposits.» Renews the instruments shine.

indicationsRenovating cleaning product for medico-surgical instrumentation. Renovating cleaning product for medico-surgical instrumentation. Renovating cleaning product for medico-surgical instrumentation. Allows the removal of organic deposits. Usable in machines, ultra-Allows the removal of organic deposits. Usable in machines, ultra-Allows the removal of organic deposits. Usable in machines, ultra-sonic tanks or manual soaking.

coMpositionPotassium hydroxide, sodium hypochlorite and deflocculating and Potassium hydroxide, sodium hypochlorite and deflocculating and Potassium hydroxide, sodium hypochlorite and deflocculating and dispersing agents.

packaging - Ref.2 cans, 5L each....................................................................................................................................10L can ............................................................................................................................................................


autoMaticdiLution oR

Information relating to the CE marking of our products and materials is included in our technical data sheets (available on demand).Information relating to the CE marking of our products and materials is included in our technical data sheets (available on demand).Information relating to the CE marking of our products and materials is included in our technical data sheets (available on demand).

Catalogue also available online

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chambre doubleaNIoS SPS PremIum

FIlTraNIoS 31dS+

aNIoSgel 85 NPc

SurFaNIoS PremIum

SurFa’SaFe PremIum

aNIoSaFe maNuclear NPc hFaaNININI

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Contents

FLOORS AND SURFACES

10 CONCENTRATED DETERGENT PRODUCTS 11 READY-TO-USE PRODUCTS 14 DISINFECTANT-DETERGENT PRODUCTS

SPRAYING AND AIRBORNE DISINFECTION

20 SPRAYING DISINFECTION 22 AIRBORNE DISINFECTION

TREATMENT OF INSTRUMENTATION

26 PRE-TREATMENT 31 HIGH-LEVEL DISINFECTION 34 EQUIPMENT

MACHINES & TUNNELS

40 DETERGENT AND DISINFECTANT-DETERGENT PRODUCTS 42 RINSING AND RESTORING PRODUCTS

HAND HYGIENE

46 CREAM AND GENTLE SOAPS 47 ANTISEPTIC SOAPS 48 HYDROALCOHOLIC GEL AND SOLUTIONS 50 EQUIPMENT

WATER FILTRATION

56 FILTERS 57 PRE-FILTRATION

SPECIAL APPLICATIONS

60 PRODUCTS FOR BEDPAN WASHERS 62 HAEMODIALYSIS GENERATORS TREATMENT 62 LAUNDRY TREATMENT

63 BIOCIDAL DIRECTIVE 64 STANDARDS GLOSSARY

Products whose formulation emerged from the latest research program (Innovative association of latest generation molecules).

This logo indicates product and material innovations recently created.

Products whose formulation includes a unique characteristic that has permitted to fi le a patent, the number of which is available on demand.

The presence of this logo certifi es a product that complies with all the criteria of our ANIOSAFE commitment.

These expert advices provide you with practical, technical and scientifi c information relating to the use of our products.

PATENTED

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Throughout this catalogue, you will fi nd different pictograms that will help you read it:

Signage of your catalogue

NEW

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FLOORS & SURFACES

THE IMPORTANCE OF BIOCLEANINGIn the hospital context, it is fundamental to make the difference between the visual cleanliness and the microbiological cleanliness.The visual cleanliness or macroscopic cleanliness represents the disappearance of soiling visible to the naked eye, including interstices, joints, anfractuosities…The microbiological cleanliness is not perceptible to the naked eye but is visible to microscope, thanks to samplings permitting the present micro-organisms identification and quantification. A surface can be macroscopically clean and support a high-count of micro-organisms.Micro-organisms survival duration on surfaces is very variable. It depends on several factors, like the germ nature, the temperature, the humidity level, the surface type and the soiling degree, especially if there is biofilm constitution.Biocleaning is the term designating the treatmentwhich groups cleaning and final application of a disinfectant product answering to the fixed objectives.Biocleaning has a qualitative action more highlightedthan the simple cleaning thanks to the chemicalaction of disinfectant products.

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TREATMENT OF FLOORS AND SURFACES

CONCENTRATED DETERGENT PRODUCTS 10 DETERG’ANIOS 10 DETERG’ANIOS SURACTIF MARINE 10 DOSING UNITS

READY-TO-USE PRODUCTS 11 ANIOS QUICK WIPES 11 LINGET’ANIOS 12 WIP’ANIOS EXCEL 12 SURFA’SAFE PREMIUM 13 ANIOS SPS PREMIUM 13 ANIOS DTS

CONCENTRATED DISINFECTANT-DETERGENT PRODUCTS 14 SURFANIOS PREMIUM 14 SURFANIOS / SURFANIOS CITRON 15 ANIOSURF ND PREMIUM

WIDE-SPECTRUM DISINFECTANT-DETERGENT PRODUCTS 16 ANIOXY-SPRAY WS 17 ANIOS OXY’FLOOR

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INDICATIONCleaning of all washable surfaces: fl oors (tiles, plastic, etc.), walls (tiles, washable paint, etc.), sanitary facilities, metal and plastic surfaces. Compatible alternately with ANIOS disinfectant products. Wetting effect, solubilising organic and inorganic stains.

COMPOSITION DETERG’ANIOSNon-ionic and anionic detergents, chelating agent, bacteriostatic and fungistatic agents, colouring and citrus fragrance.

COMPOSITION DETERG’ANIOS SURACTIF MARINEAmphoteric and non ionic surfactants, chelating agent, fragrance and colouring.

PACKAGING - REF.500 doses, 20ml each ..............................365.129 785.12912 dosing bottles, 1L each .......................365.092 785.0924 cans, 5L each + 20ml dosing pump ......365.036 785.036

INSTRUCTIONS FOR USE

CONCENTRATED DETERGENT PRODUCTS

DETERG’ANIOSDETERG’ANIOS SURACTIF MARINE » Powerful neutral detergent. » Compatible with any kind of surface. » Does not leave traces. » Available with lemon scent or marine air freshener scent.

CENTRALEPROSYSTEM COMPACTTECHNICAL CHARACTERISTICS• Dosage using VENTURI system with calibration jets.• PVC box (5 mm thick).• Connection to cold or hot water supply (55°C max).• Stainless steel bracket for 5 litre container.• Pressure resistant up to a maximum of 8 bars.• Water supply NF antipollution double-valve system.• Certifi ed Food quality washing hose.• Anti-shock gun supplied with 15 m quick coupler. Other lengths available on demand.

REF.CENTRALE PRO SYSTEM COMPACT: 1 product ....................402.015CENTRALE PRO SYSTEM COMPACT: 2 products ...................402.016

CENTRALE PREMIXTECHNICAL CHARACTERISTICS• Dosage using VENTURI system with calibration jets.• PVC box (5 mm thick).• Pressure resistant up to a maximum of 6 bars.• Connection to cold or hot water supply (60°C max).• Multiple mounting possibility through connections between plants.• Dynamic pressure: 2.5 bar.

REF.PREMIX 4.16 for bucket: 4 products, 16L/min ....................402.626PREMIX 1.16 for bucket: 1 product, 16L/min ......................402.627PREMIX 4.4 for spray: 4 products, 4L/min ..........................402.628

LEMON

SYNTHETICFRAGRANCE

MARINE

SYNTHETICFRAGRANCE

DOSING UNITS » Automatic dosing systems for cleaning

solution like DETERG’ANIOS.

PRODUCT TO BE DILUTEDi.e. 20ml for 8L

DETERG’ANIOSDETERG’ANIOSSURACTIF MARINE

For an optimized treatment of your fl oors, we advise you to alternate a detergent product with a disinfectant detergent.

Our advice

10Dangerous. Respect the precautions for use.Use with caution. Read the label and information regarding the product before each use.


READY-TO-USE PRODUCTS

ANIOS QUICK WIPES » Disinfectant wipes. » Ethanol based formula. » Wide spectrum in short time. » Aldehyde free formula. » Pleasant fragrance.

INDICATIONSANIOS QUICK WIPES are impregnated with a fast-acting disinfectant solution for non-immersible and non-invasive medical devices, previously cleaned and alcohol-resistant.

COMPOSITIONImpregnation solution: Ethanol (55%), Quaternary ammonium propionate, fragrance.

PACKAGING - REF.12 dispensers, 120 wipes each (130 x 190 mm) ...................... 2333.421

LINGET’ANIOS » Cleaning and disinfectant wipes. » Pleasant fragrance. » Wide material compatibility.

INDICATIONSCleaning and disinfection of non-immersible and non-invasive medical devices between two patients.

COMPOSITIONEthanol, chlorhexidine digluconate, aminopropyldodecylpropanediamine, synthetic fragrance, excipients.

PACKAGING - REF.1 box + 3 refi lls, 120 wipes each (130 x 190 mm) .................................. 299.3031 box + 6 refi lls, 120 wipes each (130 x 190 mm) ................................. 299.30612 refi lls, 120 wipes each (130 x 190 mm) ............................................. 299.31212 boxes, 120 wipes each (130 x 190 mm) ............................................. 299.42112 boxes, 120 wipes each (65 x 100 mm) ............................................... 299.411

Cleaning and disinfectant wipes.

Wide material compatibility.

THE IMPREGNATION SOLUTION IS:

ACTIVE AGAINST ACCORDING TO STANDARDS

BACTERIA EN 1040, EN 1276, EN 13697, EN 13727

YEASTS/MOULDS EN 1275, EN 1650, EN 13624, EN 13697

VIRUSES Active against HIV-1, Herpesvirus, HBV

THE IMPREGNATION SOLUTION IS:


BACTERIAEN 1040, EN 13727, EN 14561, EN 13697Active against MDRB according to EN 14561, EN 13697

MYCOBACTERIA EN 14348, EN 14563


VIRUSES

Active against Adenovirus, HIV-1, PRV (surrogate of HBV),BVDV (surrogate of HCV), Vaccinia virus, Herpesvirus, Coro-navirus, Rotavirus, Infl uenza virus A (H1N1), Feline Calicivirus, Norovirus MNV

INSTRUCTIONS FOR USESINGLE USE WIPES

Active from 30 sec.


Active from 1 min.

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SURFA’SAFE PREMIUM » Disinfectant detergent formulated without

alcohol, without perfume nor CMR. » Quick antimicrobial effi cacy: bacteria

including BHR, Rotavirus…from 3 min. » Quick drying, does not leave any trace. » Wide compatibility with materials, specially

polymers (polycarbonates…).


BACTERIAEN 1040, EN 13727, EN 14561, EN 13697Active against MDRB and HRB according to EN 13727, EN 13697

MYCOBACTERIA Mycobacterium terrae : EN 14348, EN 13697


VIRUSES

Adénovirus and Norovirus according to EN 14476According to EN 14476 : PRV (surrogate of HBV), BVDV (surrogate of HCV), Vaccinia virus, Herpesvirus, Rotavirus, Polyomavirus SV40

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INDICATIONSDetergent disinfectant foam, for cleaning and disinfection of surfaces, non-immersible and non-invasive medical devices (conventional ultrasound probes, cables and connectors, pressure sensors, blood sugar testers, tensiometers, refl ex hammers...) and external structures of equipments (respirators, haemodialysis generators...).

COMPOSITIONDidecyldimethylammonium chloride, excipients.

PACKAGING - REF.12 bottles, 750ml each, with foaming dispensers..........................2419.54416 bottles, 500ml each ..................................................................2419.105

Exists in wipes

WIP’ANIOS EXCEL » SURFA’SAFE PREMIUM impregnation

solution. » Formulated without CMR substances,

without perfume, nor alcohol. » 100% biodegradable viscose wipe.

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For large surfaces, preferably use the 500ml bottle.

Our advice

INDICATIONS

MORE DETAILS IN THE BROCHURE AND VIDEO


READY-TO-USEActive from 3 min.

INDICATIONSWIP’ANIOS EXCEL wipes are impregnated with a cleaning and disinfecting solution for the treatment of surfaces and medical devices.

• Cleaning and disinfection of non-immersible and non invasive medical devices (ultrasound probes, cables and connectors, pressure sensors, blood sugar testers, tensiometers...) and external structures of equipments (respirators, haemodialysis generators...).

• Wiping of endoscopy sheaths during preliminary treatment, prior to immersion for cleaning and disinfection.

PACKAGING - REF.6 sachets, 100 wipes each ...................................................................... 2446.655


Active from 3 min.




ANIOS DTS » Wetting and solubilising power. » Compatible with all washable

non-porous surfaces. » Butylglycol-free formulation. ANIOS DTS IS IDEAL FOR :

• Dry blood stains.• Interior of autoclaves.• Stainless steel surfaces.• Label glue.• Black marks on the bottom of doors (traces of wheels, shoes).• Rejuvenation of Instrubacs.• Ink, felt pen, marker, pencil, ballpoint pen, paint, lips-

tick, polish, rubber.• Diffi cult stains on textiles, before washing (care staff

overalls turned yellow).

CITRUS

FRAGRANCESYNTHETICFRAGRANCE

INDICATIONSCleaning and removal of stains from any washable surface.

COMPOSITIONAnionic surfactants, alkaline agent, glycol derivatives, synthetic fragrance.

PACKAGING - REF.12 bottles, 750ml each ......................................................2319.512


READY-TO-USE

ANIOS SPS PREMIUM » ANIOSAFE formula: based on lactic acid

and glycolic acid. » Non-corrosive product: formulated

without strong acid. » High descaling power. » Wide antimicrobial spectrum.

INDICATIONSDaily cleaning, descaling and disinfection of sanitary facilities, all enamel, stainless steel or plastic surfaces.

COMPOSITIONDidecyldimethylammonium chloride, lactic acid, glycolic acid, excipients.

PACKAGING - REF.12 foaming spray, 750ml each ...........................................2201.515



YEASTS EN 1275, EN 1650, EN 13624, EN 13697

MOULDS EN 1275, EN 13624, EN 13697

VIRUSES According to EN 14476: BVDV (surrogate of HCV), PRV (surrogate of HBV)



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SURFANIOS / SURFANIOS CITRON » Aldehyde free. » Product available since 1990. » Combination of detergent and disinfectant

action in a simultaneous operation.

INSTRUCTIONS FOR USEPRODUCT TO BE DILUTEDi.e. 20ml for 8L

INDICATIONSCleaning and disinfection of fl oors, walls and medical equipment.

COMPOSITIONN-(3-aminopropyl)-N-dodécylpropane-1,3-diamine, didecyldimethylammonium chloride, excipients.

PACKAGING - REF.500 doses, 20ml each ........................................................350.129 347.12912 dosing bottles, 1L each .................................................350.092 347.0924 cans, 5L + 20 ml dosing pump .......................................350.036 347.036

SURFANIOSSURFANIOS CITRON

CONCENTRATED DISINFECTANT-DETERGENT PRODUCTS

SURFANIOS PREMIUM » Proven effi ciency against hospital strains. » Aldehyde free, chlorine free. » Wide compatibility materials/fl oor recovering. » Optimisation of ecotoxicological information.


BACTERIAEN 1040, EN 1276, EN 13727, EN 13697, Active against MDRB according to EN 1276, EN 13697

MYCOBACTERIA Mycobacterium terrae: EN 14348, EN 14563

YEASTS EN 1275, EN 13624, EN 1650, EN 13697

MOULDS EN 1275, EN 1650, EN 13697

VIRUSESAccording to EN 14476: HIV-1, PRV (surrogate of HBV), BVDV (surrogate of HCV), Herpesvirus, Vaccinia virus, Coronavirus


BACTERIA EN 1040, EN 13727, EN 1276, EN 13697Active against MDRB


YEAST EN 1275, EN 1650, EN 13624

MOULDS EN 1275, EN 13624

VIRUSES Active against HIV-1, BVDV (surrogate of HCV), PRV (surrogate of HBV), Infl uenza virus A (H1N1)

INDICATIONSCleaning and disinfection of fl oors, walls, medical equipment and non-invasive medical devices.

COMPOSITION N-(3-aminopropyl)-N-dodecylpropane-1,3-diamine, didecyldimethylammonium chloride, excipients.

PACKAGING - REF.500 doses, 20 ml each .......................................................1917.12912 dosing bottles, 1L each .................................................1917.0924 cans, 5L + 20 ml dosing pump .......................................1917.036


Active from 15 min.

Active from 15 min.



CONCENTRATED DISINFECTANT-DETERGENT PRODUCTS

ANIOSURF ND PREMIUM » Proven effi ciency : original combination of active

substances. » Aldehyde and amphoteric-free formula. » Optimisation of ecotoxicological information.


BACTERIAEN 1040, EN 13727, EN 13697Active against MDRB and HRB according to EN 13727

MYCOBACTERIA Mycobacterium terrae EN 14348, EN 13697

YEASTS EN 1275, EN 13624, EN 13697

MOULDS EN 13624, EN 13697

VIRUSESAccording to EN 14476: PRV (surrogate of HBV), BVDV (surrogate of HCV), Vaccinia virus, Rotavirus, Herpesvirus

INDICATIONSCleaning and disinfection of fl oors, walls and medical equipment.

COMPOSITION

Didecyldimethylammonium chloride, chlorhexidine digluconate, excipients.

PACKAGING - REF500 doses, 20 ml each .......................................................2436.12912 dosing bottles, 1l each ..................................................2436.0924 cans, 5L + 20 ml dosing pump .......................................2436.036


PATENTED

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For an optimized treatment of your fl oors, we advise you to alternate a detergent product with a disinfectant detergent.

Our advice

PRODUCT TO BE DILUTEDi.e. 20ml for 8L

Active from 15 min.


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WIDE SPECTRUM DISINFECTANT-DETERGENT PRODUCTS

ANIOXY-SPRAY WS » Surface sporicidal activity. » Aldehyde free. » Does not leave traces. » Wide compatibility material/medical

devices. » Foaming spray.

INDICATIONSBroad spectrum cleaning and disinfection of surfaces, medical equipment and non-immersible and non-invasive medical devices (stethoscopes, cables and connectors, pressure sensors, blood sugar level testing material, etc.)

COMPOSITIONHydrogen peroxide (50 mg/g i.e. 5%), ethanol (91,6 mg/g) in aqueous medium.

PACKAGING - REF.6 bottles,1 litre each, with foaming spray ..........................1756.573




YEASTS EN 1275, EN 1650, EN 13624, EN 13697, EN 14562

MOULDS EN 1275, EN 1650, EN 13624, EN 13697

VIRUSESEN 14476 (Poliovirus, Adenovirus, Norovirus) Active against PRV (surrogate of HBV), BVDV (surrogate of HCV), VRS

SPORES OF BACTERIA

EN 13704Active against Bacillus subtilis according to EN 13697Active against Bacillus cereus according to EN 13697Active against Clostridium diffi cile according to EN 13697, EN 14561

ANIOXY-SPRAY WS

Wide compatibility material/medical

ALTERNATIVE TO CHLORINE.

Before every application, ensure the solution compatibility with the material : testing the product on a small surface is recommended.

Our advice

A COMPLETE SOLUTION IN THE EVENT OF AN EPIDEMIC PERIOD

Clostridium diffi cile is a positive Gram bacteria, on strict anaeroby. It is the main etiological agent implicated in the nosocomial diarrhea in adult under antibiotherapy. This bacteria develops highly resistant spores in the environment.

Since 2003, a specifi c C. diffi cile strain, named «O27», is responsible for severe and epidemic nosocomial infections. Firstly detected in Canada and in the United States of America, it was involved then in hospital epidemics in Great Britain, in Belgium and in the Netherlands. In France, where it was already isolated punctually in some hospitals, it was not identifi ed as epidemic responsible before 2006. The occurrence of digestive infection due to C. diffi cile (ICD) is the most often induced by antibiotherapy which facilitates the bacteria implantation in the alimentary canal and the secretion of two toxins (A and B) responsible of symptoms. The contamination by C. diffi cile exists by oro-faecal way and its transmission from people to people is directly done by handcarrying or from a contaminated environment.

Clostridium diffi cile but also Acinetobacter baumannii, Norovirus, Rotavirus, resistant bacteria (ERV, Enterobacteria BLSE, SARM), Tuberculosis or pneumococcus are also microorganisms responsible for hospital epidemics among young children, the elderly, and immunocompromised patients, and increase hospitalization times signifi cantly.

Infections prevention needs a reinforcement of biocleaning, with especially sporicidal disinfectant cleaning products :

» ANIOXY-SPRAY WS: Ready-to-use spray. » ANIOS OXY’FLOOR: Concentrated powder.



As a complement to ANIOS OXY’FLOOR and ANIOXY-SPRAY WS, use the airborne disinfection processAEROSEPT 500 + ASEPTANIOS AD (p. 22).

OUR ADIVCE



WIDE SPECTRUM DISINFECTANT-DETERGENT PRODUCTS

Sols et surfaces

A SIMPLIFIED PROTOCOLSave time, gain effi ciency: » A shorter treatment cycle: cleaning and full spectrum disinfection in a single

operation » Less personnel mobilised » A product stable in storage (2 years) and after preparation (8 hours) » A single dose for more simplicity: one 25g spoon or one dose in 5L of water

ANIOSAFE COMMITMENTRespect of the user » CMR, EDTA and chlorine free product » Odourless » Single dosage: prevents excessive doses

Respect of the environment » Pure and diluted product not classifi ed dangerous for the

environment (2014 data) » Perborate free formulation » Over 90% biodegradable

Respect of the equipment » Compatibility demonstrated by electrochemical protocole with

a wide range of materials: - Flooring: Tarkett®, Gerfl or® and Forbo Sarlino® brands - Stainless steel - Polymers: PVC, Corian®, etc.

A GREAT ALTERNATIVE TO CHLORINE

ANIOS OXY’FLOOR is a synergistic combination of peracetic acid and quaternary ammonium chloride in the presence of a surfactant.The peracetic acid is generated by the perhydrolysis of tetraacetylethylenediamine (TAED) by the sodium percarbonate, which limits the presence of acetic acid and hydrogen peroxide, and thus promotes better olfactory tolerance.

ANIOS OXY’FLOOR1 Step protocol

Cleaning and disinfectionwith ANIOS OXY’FLOOR 1

BLEACH3 Steps protocol

Cleaning with detergent1Rinsing2Disinfection with chlorine3 Less time,

More efficiency

INDICATIONSCleaning and broad spectrum disinfection of fl oors and surfaces.

COMPOSITIONPowder based on sodium percarbonate, tetraacetylethylenediamine and N-alkyl(C12-14)-N-benzyl-N,N-dimethylammonium chloride. Extemporaneous production of peracetic acid diluted in water. Composition in active substances for 100g of a 0.5% solution: Peracetic acid (generated in situ): approx. 750 ppm (0,75 mg/g), N-alkyl(C12-14)-N-benzyl-N,N-dimethylammonium chloride : 0.012% (0,12 mg/g).

PACKAGING - REF.100 doses, 25g each ..........................................................2131.2344 buckets, 1kg each ...........................................................2131.732


BACTERIAEN 1040, EN 13727, EN 13697, EN 14561Active against MDRB according to EN 13727, EN 13697

MYCOBACTERIA EN 14348, EN 14563, EN 13697


VIRUSES

EN 14476 (Poliovirus, Adenovirus, Norovirus)According to EN 14476: HIV-1, PRV (surrogate of HBV), BVDV (surrogate of HCV), Vaccinia virus, VRS, Rotavirus

SPORES OF BACTERIA

EN 14347, EN 13704, Active against Bacillus subtilis according to EN 13697Active against Clostridium diffi cile according to EN 13704, EN 13697

ANIOS OXY’FLOOR » Twin action : cleaning and disinfection in a simultaneous

operation. » Active against Clostridium diffi cile in 15 minutes. » Odourless powder. » Unique dose : no overdosing.

INSTRUCTION FOR USEPRODUCT TO BE DILUTEDi.e 25g for 5L

Active from 5 min.

MORE DETAILS IN THE BROCHURE AND VIDEO.


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SPRAYING AND AIRBORNE DISINFECTION

DISINFECTION OF SURFACES Disinfection of non critical surfaces in hospital is part of a significant barrier against possible infections associated to health cares. Indeed, all environmental surfaces contribute to cross contamination (contacts and exchanges between healthcare staff/surfaces/medical devices/patients). Moreover, the use of disinfectant products for the non critical surfaces treatment does not increase cost neither work. Another important point in the non critical surfaces disinfection is the contact time necessary to the action of disinfectant products. Disinfection is done after cleaning and is realised by spraying evenly a hydroalcoholic solution on surfaces. One of those solutions characteristics is a quick drying time. Thus, in adequation to this data, the action time has to be the shortest possible.

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SPRAYING DISINFECTION

SPRAYING DISINFECTION 20 ANIOSPRAY SURF 41 / ANIOSPRAY SURF 29 20 SPRAYMATIC 10S 21 ANIOSPRAY QUICK

AIRBORNE DISINFECTION 22 AEROSEPT 500 22 ASEPTANIOS AD 23 AEROSEPT 100VF 23 ANIOS DJP SF

NEW NEW

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» Bactericidal, fungicidal and mycobactericidal spectrum.

» Free of fragrance, colouring and CMR substances.

» Quick drying, leaves no traces.

» Original combination of active ingredients. » Aldehyde free. » Broad compatibility with materials and

medical devices. » Do not leave trace nor greasy fi lm.

ANIOSPRAY SURF 41

INDICATIONSDisinfection of surfaces, medical equipment and previously cleaned non-immersible and non-invasive medical devices (stethoscopes, cables and connectors, pressure sensors, blood sugar testing material...).

COMPOSITIONEthanol, N-(3-aminopropyl)-N-dodecylpropane-1,3-diamine, didecyldimethylammonium chloride, excipients.

PACKAGING - REF.12 bottles, 1L each with sprayers.........................................................2420.0734 cans, 5 litres each.............................................................................2420.034

INDICATIONSDisinfection of surfaces, medical equipment and previously cleaned non-immersible and non-invasive medical devices (stethoscopes, cables and connectors, pressure sensors, blood sugar testing material...).

COMPOSITIONEthanol, didecyldimethylammonium chloride, chlorhexidine digluconate, excipients.

PACKAGING-REF.12 bottles, 1L each with sprayers..................................................... 2421.0734 cans, 5 litres each......................................................................... 2421.034

SPRAYMATIC 10S » 10L tank, practical and compact. » Simple to operate. » Mobile and autonomous.

INDICATIONSStainless steel sprayer, mobile and pre-pressurized standalone, for disinfection of equipment and walls of operating theatres. Suitable for spraying ANIOSPRAY SURF 29 and ANIOSPRAY SURF 41.

TECHNICAL CHARACTERISTICS• Tank pressurised by compressed air• Pressure of use: 2 to 6 bars• Pneumatic type connection• Air safety valve• Flat spray nozzle

REF.SPRAYMATIC 10S ................................................................411.110

Use SPRAYMATIC 10S for treatment of large surfaces with these products.

Our advice


BACTERIA EN 1040, EN 13727, EN 13697, NF T 72-281

YEASTS EN 1275, EN 13624, EN 13697, NF T 72-281

MOULDS EN 1275, EN 13624, EN 13697

VIRUSES According to EN 14476: PRV (surrogate of HBV), BVDV (surrogate of HCV), Vaccinia virus, Herpesvirus

ANIOSPRAY SURF 29

Do not leave trace nor greasy fi lm.


BACTERIA EN 1040, EN 13727, EN 13697, NF T 72-281Active against MDRB according to EN 13697


YEASTS/MOULDS EN 1275, EN 13624, EN 13697

VIRUSESAccording to EN 14476 : Active against PRV (surrogate of HBV), BVDV (surrogate of HCV), Herpesvirus, Vaccinia virus





NEWNEW

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Information relating to the CE marking of our products and materials is included in our technical data sheets (available on demand).


ANIOSPRAY QUICK » Ethanol-based composition. » Aldehyde free. » Broad activity spectrum in 30 seconds. » Does not leave any trace. » Pleasant fragrance.

INDICATIONSQuick disinfection of surfaces, medical equipment and non-immersible and non-invasive medical devices, previously cleaned and alcohol resistant (stethoscopes, cables and connectors, pressure sensors, blood sugar testing material...).

COMPOSITIONHydroalcoholic solution (ethanol 55%), quaternary ammonium propionate, fragrance.

PACKAGING - REF.12 bottles, 1L each with sprayers.......................................2084.0734 cans, 5L each ..................................................................2084.034

Does not leave any trace.


BACTERIA EN 1040, EN 13727, EN 14561, EN 13697Active against MDRB according to EN 14561, EN 13697



VIRUSES

Active against Adenovirus, HIV-1, PRV (surrogate of HBV), BVDV (surrogate of HCV), Vaccinia virus, Herpesvirus, Coronavirus, Rotavirus, Infl uenza virus A (H1N1), Feline Calicivirus, Norovirus MNV


READY-TO-USEActive from 30 sec.

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AIRBORNE DISINFECTION

NEW

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MORE DETAILS IN THE DEDICATED BROCHURE

Aerosept 500Aerosept 500

Disinfection of non-critical surfaces plays a significant barrier role against healthcare associated infections.Airborne disinfection is an answer that is simple to implement and provides a complete antimicrobial spectrum on all previously cleaned surfaces, even the most inaccessible.

The new AEROSEPT 500 combines ergonomics and comfort of use with the proven efficacy of ASEPTANIOS AD disinfectant.

TH

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S + High treatment capacity:room from 30 to 500 m3 Process in compliance with NF T 72-281

version 2014- Bactericide and yeasticide in 30 min.- Virucide and active againstClostridium difficile in 60 min.- Fungicide and sporicide in 120 min.User-friendly operator touch screenIdentification of the room and the user via barcode

Recovery of traceability data on USB drive

LABORATOIRES ANIOSPAVÉ DU MOULIN • 59260 LILLE-HELLEMMESTÉL. +33 3 20 67 67 67 - FAX +33 3 20 67 67 68WWW.ANIOS.COM

A new innovative high performance process...

Removable nozzle

REFERENCESAEROSEPT 500.......................................................418.000ASEPTANIOS AD (4 cans, 5L each)........................2122.795

Ergonomic handle

Touchscreen

CompartmentSCAN + USB

Suction tube

Design & Ergonomy

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Airborne disinfectionmade easy

ASEPTANIOS AD

INDICATIONSFully-automated stand-alone atomiser for the disinfection of previously cleaned surfaces.

TECHNICAL CHARACTERISTICS• Tank capacity: 5L can• Average fl ow rate: 1L/hour• Empty weight: ≈ 32 Kg• Dimensions: H900 x W350 x D400• Power supply: 240/110 V – 50/60 Hz – 5 A

REF.Aerosept 500 ................................................................418.000

AEROSEPT 500 » High treatment capacity:

room from 30 to 300 m3. » Process in compliance with standard

NF T 72-281, 2014 version. » User-friendly operator touch screen. » Traceability of the room and user via barcode. » Recovery of data on USB drive.

INDICATIONSAirborne disinfection of previously cleaned surfaces and medical devices. To use in combination with AEROSEPT 500.

COMPOSITIONStabilised solution of peracetic acid (+/- 1200 ppm) and hydrogen peroxide.

PACKAGING - REF.4 cans, 5L each ..................................................................2122.795



ASEPTANIOS AD » Free of aldehyde and heavy metals. » Peracetic acid based product: prevents

corrosion. » Leaves no residue or smearing on

surfaces after aerosolization. » "0 contact" system: no risk of contact

with the product or projection.

PREVENTING NOSOCOMIAL INFECTIONS IS OUR EVERYDAY CONCERN.

Airborne disinfection is an effective solution that is easy to implement. The AEROSEPT 500 and the ASEPTANIOS AD disinfectant solution provides a full spectrum disinfection of all previously cleaned surfaces, even the most inac-cessible, avoiding the need for personnel to manually disinfect.

ACTIVE FROM

ACTIVE AGAINST ACCORDING TO STANDARDSBACTERIA NF T 72-281, EN 1040, EN 1276, EN 13697

MYCOBACTERIA NF T 72-281, EN 14348, EN 13697

YEAST/MOULDS NF T 72-281EN 1275, EN 1650, EN 13697

VIRUSES NF T 72-281, EN 14476 : Poliovirus, Adenovirus, Norovirus MNV

SPORES NF T 72-281, EN 13704

ASEPTANIOS AD - AEROSEPT 500 process: activity according to standard NF T 72-281 - 2014 version - 7ml/m3

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AIRBORNE DISINFECTION

AEROSEPT 100VF » Practical and ergonomic. » Deferred start and automatic stop. » Quicker room recovery. » Easy-to-maintain.

INDICATIONSSelf-contained, portable and fully automatic aerosol dispenser for the disinfection of previously cleaned surfaces of medical equipment.To use in combination with ANIOS DJP SF.

TECHNICAL CHARACTERISTICSAuto-regulated nozzle fl owOne-piece unit made of easy-to-maintain polyethyleneMaximum volume to be disinfected: 220 m³Average fl ow rate: 984 ml/hSealed diaphragm compressorPropeller fan: 375 m³/hTank capacity: 5 litre canUse with ANIOS DJP SF

REF.Aerosept 100 VF .................................................................417.009

AEROSEPT 100VF»»»»

INDICATIONSSelf-contained, portable and fully automatic aerosol dispenser for the disinfection of previously cleaned surfaces of medical equipment.To use in combination with ANIOS DJP SF.

TECHNICAL CHARACTERISTICSTECHNICAL CHARACTERISTICSAuto-regulated nozzle fl owOne-piece unit made of easy-to-maintain polyethyleneMaximum volume to be disinfected: 220 m³Average fl ow rate: 984 ml/hSealed diaphragm compressorPropeller fan: 375 m³/hTank capacity: 5 litre canUse with ANIOS DJP SF

REF.Aerosept 100 VF

INDICATIONSAirborne disinfection of previously cleaned surfaces and medical equipment.

COMPOSITIONChlorhexidine digluconate, didecyldimethylammonium chloride, excipients.



BACTERIAEN 1040, EN 13727, EN 13697Active against MDRB and HRB according to EN 13727, EN 13697

YEASTS EN 1275, EN 13624, EN 13697



ANIOS DJP SF » Formaldehyde free. » Bactericidal and yeasticidal spectrum. » Leaves a pleasant and fresh smell. » Wide compatibility with surfaces and

materials. » Leaves no trace nor greasy fi lm.

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THE IMPORTANCE OF PRE-TREATMENT

The pre-treatment of medical devices and medico-surgical instrumentation is a fundamental step before the cleaning operation. This step, also named pre-disinfection, requires the use of a detergent product with disinfectant properties.

The interest is multiple:• To avoid the drying of blood and proteins.• To protect care staff from any risk of contamination.• To limit cross contamination (direct "instrument/instrument or indirect "instrument/user/instrument").• To allow rejections of non contaminated solutions in the environment.

Discover our new product range issued from our latest research program "New Generation Innovation"

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PRE-TREATMENT 26 ANIOSYME PRIME / ANIOSYME FOAM 27 ANIOSYME SYNERGY 1 / ANIOSYME SYNERGY MT 27 ANIOSYME SYNERGY 5 28 ANIOS’CLEAN EXCEL D 29 ANIOSYME XL3 30 ANIOSYME PLA II 30 ANIOSEPT ACTIV

HIGH LEVEL DISINFECTION 31 ANIOXYDE 1000 32 ANIOXY-TWIN CONCENTRÉ 32 ACTANIOS HLD 33 STERANIOS 2% / STERANIOS 2% NG 33 OPASTER’ANIOS

EQUIPMENT 34 INSTRUBACS 35 MOBILE MODULES 36 MOBILE DISINFECTION RACK 36 ENDOSCOPE STORAGE CUPBOARDS 37 HDAI ENDOSCOPIC MODULE

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PRE-TREATMENT


BACTERIAEN 1040, EN 13727, EN 14561Active against MDRB and HRB according to EN 13727


YEASTS EN 1275, EN 13624, EN 14562

VIRUSESAccording to EN 14476 : HIV-1, PRV (surrogate of HBV), BVDV (surrogate of HCV), Vaccinia virus, Herpesvirus

ANIOSYME PRIME » Prevents soils from drying. » Dense foam: instruments are evenly covered. » Limits any risk of contaminated spatters. » Transportation or storage of soiled instruments prior

to treatment. INDICATIONSReady-to-use disinfectant detergent foaming spray, for transportation of instrumentation in non-humid mode or prior to machine cleaning.

COMPOSITIONQuaternary ammonium carbonate, non-ionic surfactants, enzymatic complex (protease, lipase, amylase), sequestering agents, excipients.

PACKAGING - REF.12 bottles, 750 ml each .....................................................2367.544

PATENTED

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INDICATIONSReady-to-use detergent foaming spray for transportation of instrumentation in non-humid mode or prior to machine cleaning.

COMPOSITIONNon-ionic surfactants, enzyme complexes (protease, lipase and amylase), sequestering agent, excipients.

PACKAGING - REF12 bottles, 750 ml each .....................................................2380.544


READY-TO-USE

ANIOSYME FOAM » Prevents soils from drying. » Demonstrated detergent effi cacy. » Dense foam: instruments evenly

covered. » Broad compatibility.


NEW

NEW

Recommended for transportation of instruments.

Our advice

Recommended for transportation of instruments.

Our advice

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PRE-TREATMENT

ANIOSYME SYNERGY 1 » Demonstrated detergent effi cacy from 1 minute. » Broad material compatibility. » Recommended with ANIOS high-level disinfectants.

ANIOSYME SYNERGY 5 » 5-enzymes detergent with broad-spectrum

performance. » Multi-application: soaking, ultrasonic bath, washer-

disinfector. » Effective from 1 minute in washer-disinfector. » Effective in all qualities of water (softened, mains,

etc.). » VOC-free formulation, neutral pH at dilution of use.

INDICATIONSCleaning of medico-surgical equipment, medical devices, thermosensitive instruments and endoscopic material in soaking, ultrasonic bath, automatic washing machine and washing tunnel.

ANIOSYME SYNERGY 5, with its 5 enzymes (amylase, cellulase, lipase, mannanase and protease), provides broad-spectrum performance on the ingredients of all kinds of soil.

COMPOSITIONIonic surfactants, sequestering agent, stabilising agent, enzyme complex (protease, lipase, amylase, cellulase, mannanase), excipients.

PACKAGING - REF.Use for soaking or ultrasonic bath12 dosing bottles, 1L each ......................................2235.0954 cans, 5L each + 25 ml pump ..............................2235.036Use in machine2 cans, 5L each .......................................................2235.038


TO BE DILUTEDbetween 0,05 and 0,5%

INDICATIONSCleaning of surgical and medical instrumentation, medical devices, thermosensitive instruments and endoscopic material.

COMPOSITIONNon-ionic and anionic surfactants, protease and excipients.

PACKAGING - REF12 dosing bottles, 1L each ..................... 2493.0954 cans, 5L each + 25 ml pump .............. 2493.036


PRODUCT TO BE DILUTEDi.e. 25 ml for 5L

ANIOSYME SYNERGY MT » Very strong detergent power demonstrated. » Boosted proteasic activity. » Highly effective with any quality of water. » Recommended with ANIOS high-level disinfectants.

INDICATIONSCleaning of medico-surgical equipment, medical devices, thermosensitive instruments and endoscopic equipment in soaking tank and ultrasonic bin.

COMPOSITIONNon-ionic and anionic surfactants, enzyme complex (protease, lipase and amylase), excipients.

PACKAGING - REF.12 dosing bottles, 1L each .................................................2388.0954 cans, 5L each + 25 ml pump ..........................................2388.036


PRODUCT TO BE DILUTEDi.e. 25 ml for 5L

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ANIOS’CLEAN EXCEL D » Original combination of active substances in

synergy. » High level of detergence demonstrated. » Active against MDRB and HRB. » Effective even in hard water. » Non-corrosive formulation, compatible with a

broad range of materials.

INDICATIONSCleaning and pre-disinfection of surgical and medical instruments, medical devices, thermosensitive instruments and endoscopicequipment. Collection of soiled instrumentation.

COMPOSITIONDidecyldimethylammonium chloride, chlorhexidine digluconate, non ionic and amphoteric surfactants, fragrance, colouring, excipients.

PACKAGING - REF200 doses, 25 ml each .......................................................2416.09712 dosing bottle, 1L each ...................................................2416.0954 cans, 5L each + 25 ml pump ..........................................2416.036


BACTERIA EN 1040, EN 13727, EN 14561Active against MDRB and HRB against EN 13727

MYCOBACTERIA Mycobacterium terrae : EN 14348, EN 14563

YEASTS EN 1275, EN 13624, EN 14562

VIRUSESAccording to EN 14476 : HIV-1, PRV (surrogate of HBV), BVDV (surrogate of HCV), Vaccinia virus, Herpesvirus

PATENTED

F O R MUL

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INSTRUCTIONS FOR USEPRODUCT TO BE DILUTEDi.e. 25 ml for 5L

Active from 15 min.

NEW

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PRE-TREATMENT

ACTIVE AGAINST

ACCORDING TO STANDARDS

BACTERIA EN 1040, EN 13727, EN 14561MdRB according to EN 13727

YEASTS EN 1275, EN 13624, EN 14562

VIRUSES According to EN 14476 : active against HIV-1, PRV (surrogate of HBV), Herpesvirus, BVDV (surrogate of HCV), Vaccinia virus

ANIOSYME X3 » Patented formula. » Very high performing detergency. » Optimized antimicrobial effi cacy from 5 minutes. » Non corrosive on materials.

INDICATIONSReinforced cleaning and pre-disinfection of medico-surgical instrumentation, medical devices and endoscopic equipment.Cleaning in ultrasonic bins.Collecting of soiled instrumentation.

COMPOSITIONQuaternary ammonium propionate, polyhexamethylene biguanide hydrochloride, non ionic surfactant, enzymatic complex (protease, amylase and lipase), fragrance, colouring, excipients.

PACKAGING - REF.12 dosing bottles, 1L each .................................................2633.0974 cans, 5L each + 25 ml pump ..........................................2633.095


Active from 5 min.

PATENTED

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PRE-TREATMENT

ANIOSYME PLA II » Bactericidal and fungicidal powder, active against

viruses from 15 minutes. » Compatible with any type of automatic washing

machine for medical and surgical instruments. » Tri-enzyme complex (protease, lipase, amylase). » Demonstrated detergent effi cacy (DCP*).Demonstrated detergent effi cacy (DCP*).

INDICATIONSTri-enzyme cleaning and pre-disinfection of medical devices: collecting of stained instrumentation, manual cleaning before sterilization, cleaning in ultrasonic bins, instrumentation cleaning in washing machine.

COMPOSITIONDidecyldimethylammonium chloride, non-ionic surfactant, tri-enzyme complex (protease, lipase, amylase), chelating agent, excipients.

PACKAGING-REF.100 doses, 25 g each .........................................................1307.2344 buckets, 2 kg each ..........................................................1307.0602 buckets, 5 kg each ..........................................................1307.319


BACTERIA EN 1040, NF T 72-170, EN 13727

MYCOBACTERIA Active against BK (BACTEC)


VIRUSES Active against HIV-1, PRV (surrogate of HBV), Herpesvirus, Rotavirus


Alkaline pH : check the compatibilitywith medical device.

Our advice

Double action: pre-disinfection and high-level disinfection

ANIOSEPT ACTIV » 2 in 1 powder: cleaning and high level disinfection. » Wide antimicrobial spectrum » Demonstrated detergent effi cacy (DCP*). » Shelf-life: 2 years.

INDICATIONSCleaning and disinfection of medical devices (at 0,5 or 1%). High level disinfection/cold sterilization of medical devices. Collection of stained instrumentation in ultrasonic bath.

COMPOSITIONPowder based on sodium percarbonate, tetraacetylethylenediamine and N-alkyl(C12-14)-N-benzyl-N, N-dimethylammonium chloride. Extemporaneous production of peracetic acid when diluted in water.

PACKAGING-REF4 buckets, 1 kg each ..........................................................1896.7322 buckets, 5 kg each ..........................................................1896.733

INDICATIONS


BACTERIA EN 1040, EN 13727, EN 14561Active against MDRB according to EN 13727, EN 13697



VIRUSES

Active against Poliovirus, Adenovirus and Norovirus MNV according to EN 14476According to EN 14476: active against PRV (surrogate of HBV), BVDV (surrogate of HCV), Vaccinia virus, Rotavirus, Polyomavirus SV40

SPORES OF BACTERIA

EN 14347, EN 13704 Active against Clostridium diffi cile according to EN 13704

Tests are carried out according to the European system of normalization in dirty conditions.

PRODUCT TO BE DILUTEDi.e. 25g for 5L

Active from 15 min.

INSTRUCTIONS FOR USEPRODUCT TO BE DILUTEDBetween 0,5% and 2%

Active from 5 min.

*Decreasing Cleaning Power (DCP): A methodology developped by Laboratoires ANIOS, demonstrated and reproducible, allowing to study the compared detergent effi cacy of a product.

30



HIGH-LEVEL DISINFECTION

ANIOXYDE 1000 » Broad spectrum in 5 minutes. » First high level disinfectant from PHERA® system (1998). » Alternative to glutaraldehyde. » Aldehyde free: no fi xation of proteins. » Acetic acid free. » Broad compatibility materials/medical devices. » Soaking bath stability : 14 days.

INDICATIONSHigh level disinfectant / Cold sterilant of surgical, medical, endoscopic, thermosensitive equipment and medical devices.

COMPOSITIONExtemporaneous production of peracetic acid from acetylcaprolactam (PHERA® system).ANIOXYDE 1000-GENERATOR contains 3% of hydrogen peroxide.

PACKAGING-REF4 cans, 5L each + integrated activator .................................................................. 1081.2991 box of 50 peracetic acid control test-strips ........................................................... 100.194

PATENTED

F O R M UL

A

FOR THESE PRODUCTSControl the bath conformity using a specifi c test strip.

INSTRUCTIONS FOR USEREADY-TO-USEAFTER ACTIVATION


BACTERIA EN 1040, EN 13727, EN 14561Active against MDRB according to EN 14561


YEASTSMOULDS EN 1275, EN 13624, EN 14562

VIRUSESEN 14476 (Poliovirus, Adenovirus)According to EN 14476: HIV-1, PRV (surrogate of HBV), Polyomavirus SV40

SPORES OFBACTERIA

EN 14347, EN 13704Active against Bacillus cereus according to EN 13704Active against Clostridium diffi cile according to EN 13704Active against Clostridium sporogenes according to EN 13704

Previously clean the medical device with a product like ANIOSYME XL3 or ANIOS’CLEAN EXCEL D.

Our advice

Active in 5 min.

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ANIOXY-TWIN CONCENTRÉ » Broad spectrum in 15 minutes. » Contains stabilised peracetic acid. » Aldehyde free formulation. » Concentrated product without activation reaction. » Stability of soaking bath: 24 hours. » Compatibility material/medical devices.

Concentrated product without activation reaction.

INSTRUCTIONS FOR USEREADY-TO-USEAFTER RECONSTITUTION

INDICATIONSHigh level disinfection of surgical, medical, endoscopic and thermosensitive equipment and medical devices.

COMPOSITIONActivated solution of ANIOXY-TWIN CONCENTRE containing 1200 ppm of peracetic acid.

PACKAGING-REF.12 twin-bottles...................................................................................................... 1343.4081 box of 50 peracetic acid control test-strips ........................................................ ..100.265





VIRUSESEN 14476 (Poliovirus, Adenovirus)Active against HIV-1, BVDV (surrogate of HCV),PRV (surrogate of HBV)

SPORES OF BACTERIA EN 14347, NF T 72-230/231

PATENTED

F O R M UL

A

ACTANIOS HLD » High level disinfection in 15 min. » Activity on NCTA (prions) in 30 min. » Stability of soaking bath: 14 days. » Shelf-life : 2 years. » Immediately usable after mix.

INDICATIONSHigh level disinfection of medical and surgical equipment, endoscopic and thermosensitive equipment and medical devices. Treatment of medical devices likely to be in contaminated by the prion protein (NCTA).

COMPOSITIONHydrogen peroxyde in solution with stabilizing agents.

PACKAGING-REF2 cans, 4.8L each + integrated additive 200 ml bottle ......................................... 1913.6331 box of 50 peracetic acid control test-strips ........................................................ ..100.337

Control of bath conformity using a specifi c test strip.


BACTERIA EN 1040, EN 13727, EN 14561



VIRUSES EN 14476 (Poliovirus, Adenovirus)

SPORES OF BACTERIA NF T 72-231: Bacillus subtilis

Ready to use after reconstitution

Odourless

Active in 15 min.

INSTRUCTIONS FOR USEREADY-TO-USEAFTER MIXING

Active from 15 min.

32


Dangerous. Respect the precautions for use.Use with caution. Read the label and information regarding the product before each use.Dangerous. Respect the precautions for use.Use with caution. Read the label and information regarding the product before each use.


INDICATIONSOrthophtalaldehyde based solution for treatment of thermosensitive medical devices.

COMPOSITIONOrthophtalaldehyde solution (0,55%), colouring, fragrance.

PACKAGING-REF4 cans, 5L each ................................................................................ 2504.028


BACTERIA EN 1040, EN 13727, EN 14561



VIRUSESEN 14476 : Poliovirus, Adenovirus, Norovirus MNVActive against PRV (surrogate of HBV), BVDV (surrogate of HCV), Vaccinia virus, Herpesvirus

SPORES OF BACTERIA

Active against Clostridium diffi cile O27 accor-ding to EN 14347, EN 13704

» Ready-to-use solution: absence of activator.

» Stability of soaking bath: 30 days. » Steranios 2% NG limits the evaporation of

glutaraldehyde.

STERANIOS 2% STERANIOS 2% NG


BACTERIA EN 1040, EN 13727, EN 14561



VIRUSESEN 14476 (Poliovirus, Adenovirus)Active against HIV-1, HBV, BVDV (surrogate of HBV), Herpesvirus

SPORES OF BACTERIA

NF T 72-230/231Active against Clostridium sporogenes according to NF T 72-301

READY-TO-USE


Active from 10 min.

» Ready to use solution. » Broad antimicrobial spectrum. » Control of the bath conformity

using a specifi c test strip. » Odourless. » Stability of soaking bath: 14 days.

OPASTER’ANIOS

READY-TO-USE


Active from 5 min.

INDICATIONSHigh level disinfection of medical devices, surgical, medical, endoscopic and thermosensitive equipment.

COMPOSITIONSTERANIOS 2% : 2% glutaraldehyde solution, buffered at pH 6 in the presence of surface effects catalysor, colouring, excipients.

STERANIOS 2% NG contains two compounds limiting glutaraldehyde evaporation when associated.

PACKAGING-REF4 cans, 5L each ................................................................. 382.034 ................383.034

STERANIOS 2% STERANIOS 2% NG

NEW

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EQUIPMENT

INSTRUBACS NOT SUITABLE FOR AUTOCLAVING » Soaking bins for collection of stained instrumentation.

5

SOAKING BINS NOT SUITABLE FOR AUTOCLAVE MADE IN POLYPROPYLENE» Better mechanical resistance / No edge.

LIVE VOLUME INTERNAL DIMENSIONS (LxWxH) WITHOUT TAP WITH TAP

INSTRUBAC 20L 10 L 48.5 x 27 x 17 cm 404.006 404.023

INSTRUBAC 20LSpecifi c for orthopedics

10 L 54 x 25.5 x 25 cm 404.179 -

INSTRUBAC 20Lfl at

10 L 53 x 36 x 11.5 cm 406.011 404.411


INSTRUBAC 40L 20 L 53 x 36 x 22 cm 406.012 404.412

INSTRUBAC 60 L 40 L 53 x 36 x 30.5 cm 406.013 404.413

SOAKING BINS NOT SUITABLE FOR AUTOCLAVING

5

4

2

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1

4

3

2

1

» Several tap positioning available.

INSTRUBACS FOR AUTOCLAVING » Soaking bins for collection, pre-disinfection and disinfection of

instrumentation. instrumentation.

2

4

6

5

1

3

SOAKING BINS SUITABLE FOR AUTOCLAVING + LID WITH HINGES


INSTRUBAC 1L 0,5 L 24.5 x 11 x 7.5 cm single 404.010 -

INSTRUBAC 2L 2 L 23 x 17 x 9 cm with slitwithout slit

404.038404.039

-

INSTRUBAC 4L 4 L 42 x 14 x 8.5 cm singleTwin

404.157404.158

-

INSTRUBAC 5L 5 L 36.5 x 25.5 x 9 cm single 404.002NM -

INSTRUBAC 15 L ENDOSCOPES

15 L 85.5 x 18 x 7.5 cm singleTwin

404.450404.451

404.024404.025


INSTRUBAC 20L 10 L L48.5 x l27 x H17 cm singleTwin

404.014404.019

404.021404.022

SOAKING BINS SUITABLE FOR AUTOCLAVING WITH ENVELOPING LID

1

2

3

4

5

6

» Several tap positioning available.34



EQUIPMENT

MOBILE MODULESTECHNICAL CHARACTERISTICSStailess steel mobile modules for 15L or 20L Instrubacs suitable for autoclaving.DIMENSIONSFor 15 L INSTRUBACS module: : 950 L x 440 W x 760 H mmFor 20 L INSTRUBACS module: 1022 L x 340 W x 750 H mm

REF.Module for INSTRUBAC 15 L ...............................................404.077Module for INSTRUBAC 20 L ...............................................404.020

INDICATIONSMobile module for collection of stained instruments and non-immersible equipment. Designed for use with Instrubacs 40L or 60L.

TECHNICAL CHARACTERISTICS• Stainless Steel• Dimensions : 700 L x 500 W x 710 H (mm). Height with 40L INSTRUBAC: 940 mm. Height with 60L INSTRUBAC: 1070 mm

REF.Trolley ................................................................................ 404.009

ULTRASONIC CLEANING AND IRRIGATION EQUIPMENTINDICATIONSEquipment for ultra-sonic cleaning and irrigation of hollow bodies.

TECHNICAL CHARACTERISTICS• 40L stainless steel tank• Ultrasonic power: 600 W• Power supply power: 1000 W• Puissance chauffage : 3000 W

REF.Ultra-sonic cleaning and irrigation equipment L5407 T ......404.671

For collection of the instrumentation with mobile modules, use ANIOSYME PRIME (p26).

Our advice

For collection

For soaking

DISINFECTION MOBILE MODULE

ALSO AVAILABLE

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MOBILE DISINFECTION RACKINDICATIONSThe mobile rack allows a complete irrigation of the endoscope channels with the cleaning product.

TECHNICAL CHARACTERISTICS• Autoclavable and easily detachable irrigator tubes.• A rated high-speed double channel circulation peristaltic pump.• Secure pressure by initial adjustment and adaptation of ANIOS tubes.• Electronic control with an organic LED display screen: confi guration pre-set for each channel irrigation cycle.• Optional traceability (ticket printer).

REF.Mobile disinfection rack .....................................................405.487Options : Matrix printer .....................................................................405.483Silicone pump pipes ...........................................................405.482Printer paper (10 rolls) .......................................................405.488

BUILT-IN CUPBOARDTECHNICAL CHARACTERISTICS• White built-in cupboard.• Built-in cupboard with one door or double bulkhead doors between two rooms.• Storage up to 15 endoscopes depending of the version.• Available for vertical or horizontal storage (with trays).• Retention tank.• Options: - Securit glass door. - Ventilation sytem.• Non ventilated cupboard dimensions: H 200 x W 100 x D 60 cm

ENDOSCOPE STORAGE CUPBOARDS

Ventilated cupboard with bulkhead doors

MOBILE CUPBOARDTECHNICAL CHARACTERISTICS• Beige EPOXY steel cupboard.• 10 or 15 trays, sterilizable at +134°C (trays provided).• Dimensions : - 10 endoscopes trays cupboard: External: H 190 x W 97 x D 58 cm Internal: H 160 x W 80 x D 45 cm - 5 endoscopes trays cupboard External: H 160 x W 97 x D 58 cm Internal: H 138 x W 80 x D 45 cm• Roll top closing.• Key lock.• Frame with protective bumpers.• 4 castors. 2 brakes.• 2 chromed operating handles.• Loaded PP (polypropylen) trays.

10 endoscopes horizontal mobile cupboard

BUILT-IN CUPBOARD*

Vertical storage Horizontal storage (with trays)

Non ventilated ventilated Non ventilated ventilated

double bulkhead doors

one doordouble

bulkhead doorsone door

double bulkhead doors

one doordouble

bulkhead doorsone door

Quantity of endoscopes 10 15 10 15 10

Melamine doorsGlass door

Tray (per piece)

404.511404.521

-

404.512404.522

-

404.513404.523

-

404.514404.524

-

404.515404.525404085C

404.516404.526404085C

404.517404.527404085C

404.518404.528404085C

*Quotation upon request

MOBILE CUPBOARD*

Horizontal storage(with trays)

Quantity of endoscopes 5 10

ReferencesTrays

404.088404.085C

404.085404.085C

*Quotation upon request

36



EQUIPMENT

HDAI ENDOSCOPIC MODULE » Fully automated module.

HIGH PERFORMANCE SECURITY SYSTEMS AND A QUALTY SERVICE

COMPUTER TRACEABILITYAn independent traceability system ensures that the module is operational in fail soft mode even in the event of an IT system failure. Each stage of the disinfection process is traced via an identifi cation chip dedicated to each endoscope and a badge. Full traceability is ensured via a ticket which identifi es the operator, the endoscope, the chronology of the different phases, contact times and products with its bath numbers.

PREFILTRATIONPrefi ltration on 0.5μm membrane and terminal fi ltration for 0.2μm fi lter.

VAPOURS SUCTIONEmitted by total cold disinfection solutions, using an extractor unit containing active charcoal, adapted to suit new molecules (peracetic acid).

LIQUID-TIGHTNESS TESTDetects any perforation in the endoscope tubing.

PERISTALTIC PUMP• No contact between liquid and mechanical parts.• Pressure made safe through factory adjustment.• A control touch screen.ADAPTABILITYWe advise you in your choice after studying the layout of the room, the equipment level required, the type of activity and the frequency of operations. Depending on the confi guration of your site, and to ensure optimum ease of use, the endoscopes can be processed from left to right or from right to left.

FORMATIONPersonalised protocols of use, workshops… our material department and associated services stay at your disposal for any further request.

AUTOMATED DISINFECTION OF SIPHONS

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MACHINES & TUNNELS

EFFICIENT, ECOLOGICAL, ECONOMICAL…

The performance of a washer-disinfector varies from one model to another. In most cases, correct adjustment of the product concentration, combined with a balance of other factors (water quality, instrumentation, degree of stains...), enables the cycle time and temperature to be reduced, thus saving time and energy.

Benefiting from the help of an automated treatment expert, Laboratoires ANIOS conceived a complete product range to assure you an optimum treatment of your instruments.

38

DETERGENT AND DISINFECTANT-DETERGENT PRODUCTS 40 ANIOSYME DLM MAXI / ANIOSYME SYNERGY 5 41 ANIOSYME SYNERGY WD 41 ACTANIOS LDI

RINSING AND RESTORING PRODUCTS 42 ANIOS RDA / ANIOS RN 43 ANIOS R444 / ANIOS LUB 43 ANIOS RÉNOVATEUR DMI

NEW

NEW

39Information relating to the CE marking of our products and materials is included in our technical data sheets (available on demand).

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DETERGENT AND DISINFECTANT-DETERGENT PRODUCTS

ANIOSYME DLM MAXI » Formula reinforced in detergency (kinetics

optimised). » Compatible with all types of materials

(stainless steel, titanium, synthetic, polysulphones, PVC/ABS, anodised aluminium...).

» Alkaline pH.

INDICATIONSCleaning of surgical and medical equipment and medical devices in automatic washing machines and tunnel washers.

COMPOSITIONNon-ionic and anionic surfactants, sequestering agents, enzyme complex, excipients.Specially recommended in combination with ANIOS rinsing products.

PACKAGING - REF.2 cans, 5 L each .................................................................1920.03810 L can .............................................................................1920.02425 L can .............................................................................1920.018200 L drum.........................................................................1920.005


AUTOMATIC DILUTIONbetween 0,1 et 0,5%.

Use the detergent-disinfectant foam ANIOSYME PRIME in pre-treatment (p.26).

Our advice

A complete cycle in washer-disinfector

ANIOSYME SYNERGY 5 » 5-enzymes detergent with broad-spectrum

performance. » Multi-application: soaking, ultrasonic bath,

washer-disinfector. » Effective after 1 minute in washer-disinfector. » Effective in all qualities of water (softened,

mains, etc.). » VOC-free formulation, neutral pH at use

dilution.

INDICATIONSCleaning of surgical and medical equipment, medical devices, thermosensitive instruments and endoscopic equipment in soaking, ultrasonic bath, automatic washing machine and washing tunnel. ANIOSYME SYNERGY 5, with its 5 enzymes (amylase, cellulase, lipase, mannanase and protease), provides broad-spectrum performance on the ingredients of all kinds of soil.

COMPOSITIONNon-ionic and anionic surfactants, sequestering agent, stabilising agent, enzyme complex, excipients.



PRODUCT TO BE DILUTEDbetween 0,05 and 0,5%.

PRE-DISINFECTION DETERGENCY OR DETERGENCY/DISINFECTION

RINSINGAUTOCLAVING

40

MACHINES AND TUNNELS


DETERGENT AND DISINFECTANT-DETERGENT PRODUCTS

ANIOSYME SYNERGY WD » Very strong detergent power demonstrated. » Tri-enzyme complex: effective on all kinds of

soiling. » Highly effective with any quality of water.


PRODUCT TO BE DILUTEDbetween 0,3 and 0,7%.

INDICATIONSCleaning of surgical and medical equipment, medical devices in automatic washing machine and washing tunnel.

COMPOSITIONNon-ionic and anionic surfactants, sequestering agent, stabilising agent, enzyme complex (protease, amylase, lipase), excipients.


Our adviceUse in combination with ANIOS RDA (p.42).

NEW

ACTANIOS LDI » Formula reinforced in detergency. » Recommended in the presence of

considerable organic soiling. » Alkaline pH. » Free of phosphate, EDTA, and NTA.

INDICATIONSTreatment of medical and surgical material, and medical devices in automatic washing machine and washing tunnel.

COMPOSITIONAlkaline agent, non-ionic and amphoteric surfactants, dispersing and anticorrosive agent.

PACKAGING - REF.2 cans, 5L each ..................................................................1987.36910 L can .............................................................................1987.65420 L can .............................................................................1987.271200 L drum.........................................................................1987.005


BACTERIA EN 14561

MYCOBACTERIA EN 14563

YEASTSMOULDS EN 14562

VIRUSESEN 14476 against Poliovirus, According to EN 14476: BVDV (surrogate of HCV), Vaccinia virus


PRODUCT TO BE DILUTEDbetween 0,1 et 1%.

Ensure previously about the compatibility between materials and metals with ACTANIOS LDI and all the other products used during the cleaning cycle.

Our advice

Active in 10 min.

41


Information relating to the CE marking of our products and materials is included in our technical data sheets (available on demand).Information relating to the CE marking of our products and materials is included in our technical data sheets (available on demand).

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RINSING AND RESTORING PRODUCTS

ANIOS RN » Neutralises alkaline products. » Also suitable for short cycles of

tank washing. » Complexing effect of minerals.

INDICATIONSNeutralization of alkaline residues coming from detergents and water during the washing cycle in automatic washers of medico-surgical instruments and medical devices.

COMPOSITIONFormulation based on phosphoric acid.

PACKAGING - REF.2 cans, 5L each ..................................................................193.03810L can ..............................................................................193.024


AUTOMATIC DILUTIONBetween 0,1 and 0,5%

ANIOS RDA » For a brighter instrumentation, without

trace. » Drying activator with lubricant effect. » Can be used in any quality of water

(osmotic or softened). » Highly compatible with polysulfones and

POM. » Specially designed to use in

combination with ANIOS detergents.

INDICATIONSRinsing product for medico-surgical instruments and medical devices in an automatic machine supplied with osmotic or non-osmotic water. Lubricant effect coupled with a neutralising effect on alkaline residues from detergents and water during the washing cycle. Drying activator.

COMPOSITIONCombination of non-ionic and anionic surfactants in an acid medium.

PACKAGING - REF.2 cans, 5L each ..................................................................2372.03810L can ..............................................................................2372.02425L can ..............................................................................2372.018


AUTOMATIC DILUTIONBetween 0,03 and 0,1%

NEW

HOW TO AVOID THE APPEARANCE OF TRACES?

Scale is the result of the precipitation of calcium and magnesium in hard water, helped by high temperature and pH.To avoid scale residues and traces, we recommend:

• An Intermediate Acid Rinsing (with ANIOS RN)An acid rinse neutralises alkaline residues, solubilises mineral ions contained in the water and on instruments, maintaining the instrumentation’s brilliance.

• A Final Rinsing (with ANIOS RDA)A rinsing drying activator, thanks to its sequestering and solubilising agents, helps, during the drying step, the elimination of residual water and avoids the appearance of traces resulting from mineral and scale residues contained in fi nal rinse water.

42


Dangerous. Respect the precautions for use.Use with caution. Read the label and information regarding the product before each use.Dangerous. Respect the precautions for use.Use with caution. Read the label and information regarding the product before each use.

RINSING AND RESTORING PRODUCTS

ANIOS RENOVATEUR DMI » Removes organic deposits. » Renews the instruments shine.

INDICATIONSRenovating cleaning product for medico-surgical instrumentation. Allows the removal of organic deposits. Usable in machines, ultra-sonic tanks or manual soaking.

COMPOSITIONPotassium hydroxide, sodium hypochlorite and defl occulating and dispersing agents.

PACKAGING - REF.2 cans, 5L each ..................................................................1677.50910L can ..............................................................................1677.602


AUTOMATIC DILUTION OR

ANIOS LUB » Eliminates rust pitting. » Eliminates mineral deposits. » Eliminates protein traces, iron oxide deposits and other

oxide stains.oxide stains.

INDICATIONSLubrication by soaking of articulated instrumentation.

COMPOSITIONNon-ionic surfactants, lubricating agent, preservative agents.

PACKAGING - REF.3 dosing bottles, 1L each ...................................................883.137

ANIOS R444 » Eliminates rust pitting, protein traces, iron oxide

deposits and other oxide stains. » Eliminates mineral deposits. » Soaking method: integrated dosing system. » Compatible with any quality of dilution water.

INDICATIONSA specifi c renovation product for stainless steel instruments and medical devices. Removes protein traces, iron oxide deposits and other oxide stains.

COMPOSITIONPhosphoric acid, non-ionic surfactants.

PACKAGING - REF.3 dosing bottles, 1L each ...................................................191.137

Usable in ultrasonic bin


PRODUCT TO BE DILUTED0.5 to 5% i.e. 5 to 50ml for 1L


PRODUCT TO BE DILUTED2.5% i.e. 25ml for 1L

PRODUCT TO BE DILUTED0.4 to 1% i.e. 4 to 10ml for 1L

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HAND HYGIENE

SURGICAL HAND DISINFECTION BY FRICTION

Surgical hand disinfection by friction was previously named « surgical antisepsis of hands » because the European standards were not yet published. It started in 1995 in France and then was confirmed in 1999 with the edition of the guidelines “100 recommendations for surveillance and prevention against nosocomial infections”. The north-American guidelines, published in 2007, reclaim the importance of hand disinfection in prevention for pathogenic agents’ transmission. Since 2006, the W.H.O. edited guidelines with the slogan “Clean care is safer care” pushing ahead hand disinfection. Many publications highlight advantages linked to hydroalcoholic products use, in terms of tolerance, observance and cost. The formula of hydroalcoholic products and their components results in those advantages.Today, the technique evolved toward a “good procedure” described in 7 steps in the guidelines of 2009 and hand rubbing is an indicator for the fight against nosocomial infections. Many studies realised in hospitals allow to connect the MRSA level decreasing to the hydroalcoholic products consumption.

44

HAND HYGIENE

CREAM AND GENTLE SOAPS 46 CRÈME PROTECTRICE 46 ANIOSAFE MANUCLEAR NPC HF 46 ANIOSAFE SAVON DOUX HF

ANTISEPTIC SOAPS 47 DERMANIOS SCRUB CG 47 DERMANIOS SCRUB CHLORHEXIDINE 4% 47 DERMANIOS SCRUB POVIDONE IODINE

HYDROALCOHOLIC GEL AND SOLUTIONS 48 ANIOSGEL 85 NPC / ANIOSRUB 85 NPC 49 ANIOSGEL 800 / ANIOSRUB 800

EQUIPMENT 50 COUCOU BOX / GEL DISPENSER TOTEM 51 WASHBASINS 53 DISPENSERS AND HOLDERS

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CREAM AND GENTLE SOAPS

» Without detergent agents, nor fragrance and colouring. » Enriched in moisturizing susbtance. » Adapted to sensitive skins and for frequent use. » Preservation of the product demonstrated according to

NF EN ISO 11930.

INSTRUCTIONS FOR USEWash for 30 seconds. Rinse. Dry thoroughly.

» Without detergent agent. » Enriched in moisturizing susbtance. » Preservation of the product demonstrated according to

NF EN ISO 11930.

ANIOSAFE SAVON DOUX HFINDICATIONSRecommended for frequent hand hygiene and general body cleansing in hospital.

INGREDIENTSAqua (Water), Disodium Lauroamphodiacetate, Sodium Lauryl Sulfate, Hexylene Glycol, Glycerin, Linoleamide DEA, Disodium Ricinoleamido MEA-Sulfosuccinate, Benzyl Alcohol, Sodium Benzoate, PEG-200 Hydrogenated Glyceryl Palmate and PEG-7 Glyceryl Cocoate, Parfum (Fragrance), Lactic acid.

PACKAGING - REF.12 bottles, 500ml each, with screwed pump ......................1918.22812 bottles, 500ml each, for dispenser ................................1918.11012 bottles, 1L each, with screwed pump ............................1918.22912 airless bottles, 1L each .................................................1918.1444 cans, 5L each ..................................................................1918.034

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DERMATOLOGICALLY TESTED

ANIOSAFE MANUCLEAR NPC HF

Find our dispenser range p.53

1 PUMP SQUIRT

INDICATIONSRecommended for frequent hand hygiene and general body cleansing in hospital.

INGREDIENTSAqua (Water), Cocamidopropyl Betaine, Glycerin, Sodium C14-17 Alkyl Sec Sulfonate, PEG-200 Hydrogenated Glyceryl Palmate (and) PEG-7 Glyceryl Cocoate, Benzyl Alcohol, Sodium Benzoate, Sodium Chloride, Lactic acid.

PACKAGING - REF.24 bottles, 250ml each ......................................................1921.11712 bottles, 500ml each, with screwed pump ......................1921.22812 bottles, 500ml each, for dispenser ................................1921.11012 bottles, 1L each, with screwed pump ............................1921.22912 airless bottles, 1L each .................................................1921.1445L can ................................................................................1921.034

1

23

INSTRUCTIONS FOR USEWash for 30 seconds. Rinse. Dry thoroughly.

1 PUMP SQUIRT

CRÈME PROTECTRICE » Formula without paraben. » Non greasy concentrated formula. » Penetrates and takes effect quickly. » Contains glycerine and shea butter.

INDICATIONSGlycerin and shea butter present in the CRÈME PROTECTRICE bring the essential ingredients to protect hands irritated by the stresses and strains of daily life (descaling agents, solvents, etc…).

INGREDIENTSAqua (Water), Glycerin, Cetearyl Alcohol, Sodium Cetearyl Sulfate, Cyclopentasiloxane, Butyrospermum Parkii (Shea) Butter, Cyclohexasiloxane, Triethanolamine, Sodium Benzoate, Stearic Acid, Levulinic Acid, Parfum (Fragrance), p-Anisic Acid, Sodium Levulinate, o-Cymen-5-ol, Hexyl Cinnamal, Benzyl Benzoate, Benzyl Salicylate, Linalool, Citronellol, Hydroxycitronellal, Butylphenyl Methylpropional, Hydroxyisohexyl 3-Cyclohexene Carboxaldehyde.

PACKAGING - REF.50 bottles, 50ml each ..........................................399.75650 tubes, 100ml each ..........................................399.37212 bottles, 500ml each with screwed pump .........399.236

123

INSTRUCTIONS FOR USEPour about 1ml on clean and dry skin. Massage hands without forgetting the palm and nails. Wait until dry.

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3DERMATOLOGICALLY

TESTED

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3DERMATOLOGICALLY

TESTED

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46

HAND HYGIENE


HAND HYGIENE

ANTISEPTIC SOAPS


DERMANIOS SCRUB CHLORHEXIDINE 4% » Chlorhexidine based formulation. » Hygienic handwash : 3ml / 30 sec (EN 1499). » Surgical handwash : 2 x 3 ml / 5 min (EN 12791).


BACTERIA EN 1040, EN 13727Active against MDRB according EN 13727

YEASTS EN 1275, EN 1650

VIRUSESAccording to EN 14476 : HIV-1, PRV (surrogate of HBV), BVDV (surrogate of HCV), Vaccinia virus, Herpesvirus, Rotavirus, VRS

STANDARDS OF APPLICATION

Hygienic handwash: EN 13727, EN 1499Surgical handwash: EN 13727, EN 12791

30ML VERSION FOR THE PATIENT’S

SHOWER

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2

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INDICATIONSAntiseptic soap for hygienic and surgical handwash. Washing and disinfection of the whole body.

COMPOSITIONChlorhexidine digluconate, excipients.

PACKAGING - REF.100 bottles, 30ml each ......................................................2173.76612 bottles, 500ml each with screwed pump .......................2173.270 12 bottles, 1L each with screwed pump .............................2173.38512 airless bottles, 1L each .................................................2173.1444 cans, 5L each ..................................................................2173.028

123

INSTRUCTIONS FOR USEHygienic handwash: 3ml / 30 sec.Surgical handwash: 2 x 3ml / 5 min.Rinse and dry thoroughly.



DERMANIOS SCRUB CG » Hygienic Handwash: 3ml/30 seconds. » Broad antimicrobial spectrum, including against

MDRB.

DERMANIOS SCRUB DERMANIOS SCRUB DERMANIOS SCRUB DERMANIOS SCRUB

» Broad antimicrobial spectrum, including against MDRB.

2

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4

INDICATIONSAntiseptic soap for hygienic handwash and general body cleansing in case of MRSA and multi-drug resistant bacteria contamination.

COMPOSITIONChlorhexidine digluconate, washing agents, foaming agent and thickening agent.

PACKAGING - REF.12 bottles, 500ml each, with screwed pump ......................2082.52212 bottles, 500ml each for dispenser .................................2082.11012 bottles, 1L each, with screwed pump ............................2082.52312 airless bottles, 1L each .................................................2082.1444 cans, 5L each ..................................................................2082.034

INSTRUCTIONS FOR USEHygienic handwash: 3ml/30 sec.Surgical handwash: 2x3ml/5min.Rinse and dry thoroughly.

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BACTERIAEN 1040, EN 13727, EN 1499Active against MDRB

YEASTSMOULDS EN 1275, EN 1650

VIRUSES Active against BVDV (surrogate of HCV), Herpesvirus, RSV

DERMANIOS SCRUB POVIDONE IODINE » Formulation based on polyvinylpyrrolidone.


BACTERIA EN 1040, EN 13727

YEASTS EN 1275, EN 13624

STANDARDS OF APPLICATION Hygienic washing: EN 13727, EN 1499

INDICATIONSPre-operative washing and disinfection of the entire body.Hygienic handwash (EN 1499).

COMPOSITIONPovidone iodine, excipients.

PACKAGING - REF.Pre-operative shower:100 bottles, 30ml each .......................................206.419Handwashing:12 bottles, 500ml each, with screwed pump .......206.2704 cans, 5L each ...................................................206.028

INSTRUCTIONS FOR USEHygienic handwash: Pour 1 dose (3 ml) and wash the hands and wrists for 1 minute. Rinse and dry thoroughly.

1

2

30ML VERSION FOR THE PATIENT’S

SHOWER

2

1READY-TO-USEActive from 1 min.

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HYDROALCOHOLIC GEL AND SOLUTIONS

ANIOSGEL 85 NPC » Hypoallergenic formula. » No allergenic substance, no fragrance, no colouring. » Broad antimicrobial spectrum in 30 sec. » Hygienic treatment in 30 sec (EN 1500). » For hygienic treatment and surgical disinfection.

TESTED UNDER DERMATOLOGICAL CONTROL: HYPOALLERGENIC FORMULA

123456

PACKAGING - REF.20 bottles, 75ml each ........................................................1644.2746 bottles, 300ml each with screwed pump .........................1644.36612 bottles, 500ml each with screwed pump .......................1644.63612 bottles, 500ml each for dispenser .................................1644.63912 bottles, 1L each with screwed pump .............................1644.63712 airless bottles, 1L each .................................................1644.638500 doses, 3ml each ..........................................................1644.273100 doses, 30ml each ........................................................1644.651

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INDICATIONSHygienic treatment and surgical disinfection of hands by rubbing.

COMPOSITIONEthanol in the presence of thickening, moisturizing and emollient agents, and water.

ANIOSRUB 85 NPC

Liquid version

ALSO AVAILABLE

A COLLABORATION WITH W.H.O.PRIVATE ORGANIZATIONS FOR PATIENT SAFETY

Laboratoires ANIOS is since May 2012 a member of the Private Organizations for Patient Safety (POPS), a program that has been launched by W.H.O. and groups private industry companies specialized in hand hygiene with one aim : harness industry strengths to align and improve implementation of W.H.O. recommendations for patients security. This collaboration has as sole objective the reduction in health-care associated infections through improvements in hand hygiene in different parts of the world, including in least developed countries.

ALSO AVAILABLE


BACTERIA EN 1040, EN 13727Active against MDRB and HRB according to EN 13727


YEASTS/MOULDS EN 1275, EN 13624

VIRUS

EN 14476 (Poliovirus, Adenovirus, Norovirus)According to EN 14476: HIV-1, PRV (surrogate of HBV), BVDV(surrogate of HCV), Rotavirus, Herpesvirus, VRS, Infl uenzavirus A H5N1 and H1N1.Active against Coronavirus.

PROTOCOLE STANDARDS CONDITIONS

HYGIENIC HANDWASH EN 13727, EN 1500Enough quantity to keep wet hands during 30 seconds

SURGICAL HANDWASH EN 13727, EN 12791Enough quantity to keep wet hands during 2 x 45 seconds


1.5 ml Pump

48

HAND HYGIENE


HAND HYGIENE

HYDROALCOHOLIC GEL AND SOLUTIONS

TESTED UNDER DERMATOLOGICAL CONTROL: HYPOALLERGENIC FORMULA

ANIOSRUB 800

Liquid version

ALSO AVAILABLE

ANIOSGEL 800 » High level of observance. » Tested under dermatological control. » Hypoallergenic formula. » Adapted to sensitive skins. » Preserves the hydration of the skin. » Broad antimicrobial spectrum from 30 sec. » Conform to latest european standards.

INDICATIONSHygienic treatment and surgical disinfection of hands by rubbing.

COMPOSITIONEthanol in the presence of thickening, moisturizing and emollient agents, and water.

PACKAGING - REF.20 bottles, 75ml each ........................................................2550.2746 bottles, 300ml each with screwed pump .........................2550.76212 bottles, 500ml each with screwed pump .......................2550.74812 bottles, 500ml each for dispenser .................................2550.63912 bottles, 1L each with screwed pump .............................2550.76312 airless bottles, 1L each .................................................2550.333100 doses, 30ml each ........................................................2550.651

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NEW

NEW


BACTERIAEN 1040, EN 13727Active against MDRB et HRB according to EN 13727 (K. pneumonia, OXA 48, E. coli OXA 48, E. cloacae OXA 48, S. aureus SARM)



VIRUSEN 14476 (Poliovirus, Adenovirus, Norovirus MNV)According to EN 14476: BVDV (surrogate of HCV), PRV (surrogate of HBV), HIV-1, Rotavirus, Herpesvirus

PROTOCOLE STANDARDS CONDITIONS

HYGIENIC TREATMENT EN 1500Enough quantity to keep hands wet during 30 seconds

SURGICAL TREATMENT EN 12791Enough quantity to keep wet hands during 2 x 45 seconds

MORE DETAILS IN THEDEDICATED BROCHURE

Perfo r m anc e

Toler a n c e O bser van ce

SOFTNESS AND PERFORMANCE

1

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4


3 ml Pump


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TRAINING TOOLS

COUCOU BOX » Equipment for the validation of standardised techniques

application for handrubbing with hydroalcoholic gel and solutions.

DESCRIPTION OF THE SYSTEMThanks to a phosphorescent agent contained in a hydroalcoholic product especially designed for this application, the user visualizes with the trainer the handrubbing quality.

TECHNICAL CHARACTERISTICSSIZE : L 52 cm x D 41 cm x H 40 cmDESCRIPTIONMade from highly-resistant high-pressure PVC material.The equipment features a carrying handle and dual viewing (user/trainer).POWER SUPPLY:230V single phase + PE 50 Hz / Power: 70 VA.Via a standardized plug 10/16 A 230 V single phase + PE 50 Hz, protected by a residual current device of 30 mA max.ELECTRICAL ELEMENTS:• 1 ultraviolet tube 8 W.• 1 male plug 2 poles +PE, with 5 x 20 mm fuses (315 mAT) and switch.• 1 mains cable 2 poles +PE.• 1 strip for a fl uorescent 8 W tube.

PACKAGING - REF.COUCOU BOX.....................................................................................425.044COUCOU BOX with cam .....................................................................425.044LCDANIOSGEL 85 NPC fl uorescent - 6 bottles, 300 ml each.....................1759.762

IDEAL FORTRAININGS

INSIDE VIEW:the areas where the gel was applied are unveiled by the UV lamp

GEL DISPENSER TOTEM » Anti-drop system included. » Electronic dispenser included. » Already mounted.

INDICATIONSAims to provide alcoholic gel for everyone in your establishment. Mobile with it’s electronic battery-powered dispenser, the panel can be installed in every room, to allow the public to disinfect their hands under all circumstances.

REF.Gel dispenser totem ...........................................................425.124Delivered with an electronic ABS dispenser for 1L Airless bottles and an anti-drop holder. Delivered in individual boxes.

ANIOSGEL 85 NPC with fl uoresceine (300 ml bottle) is specially designed to be used with the training box.

50

HAND HYGIENE


HAND HYGIENE

WASHBASINS

ANIOSAVE WASHBASIN 1 UNIT » Autonomous (no power supply needed). » A one-piece design for perfect hygiene. » Electronical distribution of water.

INDICATIONSFor simple handwash with or without terminal fi ltration.

TECHNICAL CHARACTERISTICS• Water distribution by electronical infrared proximity detector.• Elbow-controlled soap dispenser.• Temperature adjustment by premix.• Pre-fi ltration in option (300 µm).

REF.Washbasin without fi ltration system ..................................408.250(no pre-fi lter nor terminal fi lter)Washbasin equipped with a fi ltration system .....................408.200(with pre-fi lter 300μm, regulator valve, quick release connector, FILTRANIOS 31DA+ terminal fi lter)

• 800 W x 510 D x 705 H (mm).• Weight : 12 kg.• Power supply: Long-lasting 6V battery.

A WIDE RANGE OF WASHBASINS TO CATER FOR ALL NEEDS

Complying with the recommendations of the M.S.G. / C.L.*, our washbasins meet all of your requirements. Practical, easy to maintain, ergonomic, fi nal fi ltration… for every need there’s an ANIOS washbasin.

*M.S.G. / C.L. : Market Study Group of Care Centers and Laboratories devices

MORE DETAILS IN OUR SPECIFIC BROCHURE AVAILABLE ON REQUEST.

Superfi cial and intensive careEndoscopyConsultation roomsLocker roomsMaternity hospitals and nursing homesPackaging and storage roomsShared kitchens

Ideal for the following environments:

CHOOSE THE READY-TO-USE WASHBASIN!


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WASHBASINS

COMPACT WASHBASIN 2 UNITS » Autonomous (no power supply needed). » Easy to maintain : no retention area. » Electronical distribution of water.

INDICATIONSFor simple handwash.

TECHNICAL CHARACTERISTICS• Water distribution by electronical infrared proximity detector.• Elbow-controlled soap dispenser.• Temperature adjustment by premix.• Pre-fi ltration in option (0,5 µm)

REF.Washbasin without fi ltration system ..................................423.270(no pre-fi lter nor terminal fi lter)Washbasin equipped with a fi ltration system .....................423.220(with pre-fi lter 0,5 μm, regulator valve, quick release connector, FILTRANIOS 31DA+ terminal fi lter)


Superfi cial careIntensive careEndoscopyLocker roomsConsultation roomsPackaging and storage roomsMaternity hospitalNursing homesShared kitchens


HYPERASEPTIC WASHBASIN 2 UNITS » Autonomous (no power supply needed). » Headboard included. » Ergonomy and tank fi tted to surgical washing. » Easy to maintain : no retention area. » Electronical distribution of water.

INDICATIONSFor simple or surgical handwash.

TECHNICAL CHARACTERISTICS• Water distribution by electronical infrared proximity detector.• Elbow-controlled soap dispenser.• Temperature adjustment by premix.• Quick connection to fi t FILTRANIOS+ on outlet of each swan neck.

REF.Washbasin without pre-fi ltration system ............................423.370(no pre-fi lter 0,5μm)Washbasin equipped with a fi ltration system .....................423.320(with pre-fi lter 0,5 μm, regulator valve, quick release connector, terminal fi lter FILTRANIOS 31DA+ terminal fi lter)


Operating theatresAseptic areas


52

HAND HYGIENE


HAND HYGIENE

DISPENSERS AND HOLDERS

DISPENSERS AND HOLDERS FOR BOTTLES WITH SCREWED PUMP

HOLDERS SUITABLE FOR BED

DISPENSERS FOR 1L AIRLESS BOTTLES

For b

ottle

For b

ottle

WALL-OFF HOLDERREF. 425.058

PUSH-BUTTONCONTROLLED ABS DISPENSERREF. 425.107

ELECTRONICALLY CONTROLLED ABS DISPENSERREF. 425.157

For b

ottle

STAINLESS STEEL ELBOW-CONTROLLED DISPENSERREF. 425.022

PVC ELBOW-CONTROLLED DISPENSERREF. 425.045

For b

ottle


For b

ottle

PVC ELBOW-CONTROLLEDDISPENSERREF. 425.092

For b

ottle

PVC ELBOW-CONTROLLEDDISPENSERRÉF. 425.091


For b

ottle

For b

ottle

300ML 500MLDiam. 16/23 mm 425.104 425.110Diam. 23/32 mm 425.105 425.121Diam. 32/42 mm 425.106 425.122

For b

ottle

300ML 500ML 1L425.251 425.250 425.249

ANTI-DROP SYSTEM FOR 1L AIRLESS DISPENSERSREF................................ 425.109

FIXATION ON HEADBOARDSFIXATION ON A BAR

For b

ottle


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WATER FILTRATION

PRE-FILTRATION OF WATER

The setting up of pre-filters upstream from a terminal 0.22μm filter allows to optimise water filtration results, preserving the terminal 0.22μm filter longevity (delay of filtering membrane bloc-kage and maintaining of a constant filtered water flowrate).

Indeed, many contaminants, soluble or insoluble, exist in water: solid materials in suspension sedi-menting (clays, gypsum, rust…) or not (colloids), alive materials (bacteria, microalgae, viruses…)

The Fouling Index test permits to assess the qua-lity of the water to be filtered by determining the water blockage index and identifying the contami-nants present in water.

54

WATER FILTRATION

FILTRATION 56 FILTRANIOS 31 DA+ / FILTRANIOS 31 DS+ 57 FILTRANIOS 31 LPS+ / FILTRANIOS 2W A

PRE-FILTRATION 57 PRE-FILTERING UNIT

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FILTRANIOS

ECO DESIGN• Filtration area calculated to fi lter

just the amount of water necessary for use.

• Optimisation of fi lters’ weight (e.g. 100 g for the FILTRANIOS 31 DA+): less processed materials, reduced quantity of waste.

• These fi lters are designed without undesirable additives (epoxy derivatives, bisphenol A (PBA), Dioxin, Latex, Lactose, Phthalate (DEHP), Plasticisers, Silver salts, Abestos, Polychlorobiphenyls (PCB), Melamine).

• Reduced volume of outer packa-ging: Optimised packaging volume to limit the environmental impact of transport.

FULL TRACEABILITY• 2 traceability labels on the bag,

of which one can be detached and repositioned to document the tracking log.

• 1 traceability label kept on the fi lter recording the dates of fi tting and removing the fi lter.

• Printing on the fi lter.

FILTRANIOS 31 DA+ » Retention of all germs

INDICATIONSA disposable sterile fi lter, it removes all germs and water mycoplasma. Ideal for hygienic and surgical handwash and rinsing of medical devices such as endoscopic equipment after high level disinfection.

REF.CPC connector - Shower head outlet ..............................................432.173Walther connector - Shower head outlet .........................................432.174CPC connector - Straight outlet......................................................432.177Walther connector - Straight outlet ................................................432.178CPC connector - CPC outlet ...........................................................432.180

FILTRANIOS 31 DS+ » Retention of all germs

INDICATIONSA disposable sterile fi lter, it removes all germs and water mycoplasma. Ideal for patients shower and bath in healthcare services, high-risk services, burns unit and imunodepressed patients.

REF.Shower head fi lter 31DS+ ................................. 432.175

31DAYS

COMPOSITION OF FILTER MEDIA• 1 pre-fi ltration layer of polypropylene, with «funnel

effect» density gradient.• 2 asymmetrical membranes (1 membrane for

FILTRANIOS 31 LPS+) of PolyEtherSulphone (PES).

A UNIQUE DESIGN

Walther and CPC connectors available.Protective skirt.Straight, shower head and threaded outlets available.

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1

2

3 Prefi ltration Polypropylene 3 μm with density gradient (10 μm to 3 μm).Retention effi ciency: 100% at 3 μm; 98% at 1 μm

0.2 μm validated asymmetrical membrane of PolyEtherSulphone

UPSTREAM

DOWNSTREAM

FILTRANIOS 31 LPS+ (page 57)

UPSTREAM

DOWNSTREAM

Prefi ltration Polypropylene 1 μm with density gradient (5 μm to 1 μm).Retention effi ciency: 100% at 1 μm; 98% at 0.5 μm

0.2 μm validated asymmetrical membrane of PolyEtherSulphone

0.1 µ m validated asymmetrical membrane of PolyEtherSulphone

FILTRANIOS 31 DA+, 31 DS+

31DAYS

56

WATER FILTRATION


WATER FILTRATION

FILTRANIOS

14DAYS

FILTRANIOS 2W A » Retention of all germs

INDICATIONSWater fi ltration (retention of all germs) for hygienic and surgical handwash, rinsing of medical devices such as endoscopic equipment after high level disinfection…

REF.Walther connector - Shower head outlet ............ 432.441Walther connector - Straight outlet ................... 432.442 CPC connector - Shower head outlet ................. 432.443CPC connector - Straight outlet......................... 432.444

TECHNICAL CHARACTERISTICS FILTRANIOS 2W A

PRE-FILTRATION LAYER Polypropylene 1 μm

2 MEMBRANES PolyEtherSulphone 0.2 μm

SUPPORT AND DRAINING LAYERS Polypropylene

CAPSULE BODY Polypropylene

EFFECTIVE FILTRATION AREA 2 x 425cm²

FILTRATION FLOWRATE

3 bar : 6,5 L/min.

MAXIMUM CONDITIONS OF USE 5 bar/+50°C

CHIMICAL RESISTANCE > 1000 ppm active chlorine

INLETS / OUTLETS AVAILABLE

Inlets : Walther / CPCOutlets : Shower head / Straight

HEIGHT 74 mm

WEIGHT 100 grammes

PRE-FILTERING UNITFOR SINGLE-USE FILTERSInstalled upstream from the disposable fi ltering system, retains particles of 0,5 μm and over, guaranteeing optimum use of FILTRANIOS 31DA+, 31DS+, 31LPS+ and 2W A.

INCLUDES• One polypropylene case.• One 0,5 μm pre-fi ltering sleeve.• One pressure reducing valve with pressure controlling manometer.

FILTRANIOS 31 LPS+ » Retention of Legionella

INDICATIONSA disposable sterile fi lter, specially designed for the retention of Legionella. Ideal for patients shower and bath in healthcare services, high-risk services, burns unit and immunodepressed patients.

REF.Showerhead fi lter 31LPS+ ................................. 432.176

31DA+ 31DS+ 31LPS+

PRE-FILTRATION LAYER1 μm polypropylene with «funnel effect»

density gradient from 5 μm to 1 μm

3 μm polypropylene with «funnel effect»

density gradient from 10 μm to 3 μm

MEMBRANE ”Select pleated” conception 1 high-capacity asymmetrical PES 0.2 μm membrane,

1 PES asymmetrical 0.2 μm membrane

SUPPORT AND DRAINAGE LAYERS

Polypropylene

FILTER BODY Polypropylene

FILTRATION SURFACE 410cm2 500cm2

FILTRATION FLOW RATE 5 litres/minute at 3 bar 6,5 litres/minute at 3 bar 14 litres/minute at 3 bar

MAXIMUM CONDITIONS OF USE 5 bar at +60°C (for 31 days) + 1 cycle at +70°C for 30 minutes.

CHEMICAL RESISTANCE Active chlorine: > 1000 ppm at +40°C - APA: 250 ppm at +40°C for 31 days

DIMENSIONSHeight: 89 mm

ø cartridge: 76 mm ø shower head: 54 mm

Length: 222 mm - Height: 68 mmø shower head: 80 mm

WEIGHT 100 grammes 175 grammes

31DAYS


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58


PRODUCTS FOR BEDPAN WASHERS 60 ANIOS LB 20 / ANIOS LB 30 / ANIOS LB 40 61 ANIOS LB 200 / ANIOS LB 300 / ANIOS LB 400

HAEMODIALYSIS GENERATORS TREATMENT 62 OXY-ANIOLYSE 9000

LAUNDRY TREATMENT 62 STERILINGE SA / SOUPLANIOS

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PRODUCTS FOR BEDPAN WASHERS

ANIOS LB 30

PACKAGING - REF2 cans, 5L each ........................2163.038


ANIOS LB 20 ANIOS LB 40


THE DIVERSITY OF BEDPAN-WASHERS EXISTING ON THE INTERNATIONAL MARKET INVOLVESTHE USE OF PRODUCTS SPECIFICALLY MADE.FIND OUR 6 PRODUCTS DESIGNED FOR YOUR EQUIPMENTS IN PLACE.

FIND MORE ABOUT OUR BEDPAN RANGE IN OUR DEDICATED BROCHURE, AVAILABLE ON REQUEST.

NeutralANIOS LB 30about 2,00

ANIOS LB 40about 2,20


» High solubilizing power of calcium salts and magnesium.

» Contains surfactants for easier drying. » Chelating formula without EDTA, NTA nor

phosphate.

CHARACTERISTICSAcid rinsing products for treatment in thermal bedpan washers.Compatible with bedpans, urine bottles made of glass, stainless steels and plastics.

AUTOMATIC DILUTIONi.e. 0,5 to 5ml/L


pH SCALE

ACID

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ANIOS LB 400


ANIOS LB 300

PACKAGING - REF4c ans, 5L each ........................2160.034

ANIOS LB 200


PRODUCTS FOR BEDPAN WASHERS

ANIOS LB 300about 13,40Neutral



» Chelating power in low alkaline media. » Can be used in any quality of water (tap

water or treated water). » Phosphate free, without EDTA nor NTA. » Rinsing effect for an easier drying.

CHARACTERISTICSChelating detergent products with low alkaline pH, for the treatment in thermal bedpan-washers. Compatible with bedpans, urine bottles made of glass, stainless steels and plastics.

AUTOMATIC DILUTIONi.e. 1 to 3ml/L


ALKA

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HAEMODIALYSIS GENERATORS TREATMENT

OXY-ANIOLYSE 9000 » Compatible with all sensitive materials from dialysis

equipment. » No descaling cycle requested. » Peracetic acid solution with reinforced descaling

power. » Broad antimicrobial spectrum. » Methods to analyse traces of both active compounds in

rinsing waters, using teststrips, available on request.

INDICATIONSDisinfection of haemodialysis generators and circuits and disinfection of water treatment systems.

COMPOSITIONStabilized solution of peracetic acid and hydrogen peroxide. Peracetic acid : 1%.

PACKAGING - REF.4 cans, 5L each ............................................................................1610.18525L can ........................................................................................1610.010Testing strips of H2O2 level (box of 100) .........................................100.344

INSTRUCTIONS FOR USEAutomatic dilution during automated treatment. Optimum contact time : 20 to 30 minutes.

SOUPLANIOS » Laundry softener. » Active against bacteria, yeasts and

moulds. » Soften your laundry after the washing

cycle.

STERILINGE SA » Disinfection of contaminated laundry » Active against bacteria, yeasts,

moulds and viruses. » Controlled foaming power. » Soaking in cold or hot water.


BACTERIA EN 1040, EN 13727, EN 14561

MYCOBACTERIA Mycobacterium terrae: EN 14348, EN 14563Mycobacterium avium: EN 14348


VIRUSESEN 14476 (Poliovirus)Active against HIV-1, PRV (surrogate of HBV), BVDV (surrogate of HCV), Herpesvirus

SPORES NF T 72-230 (Bacillus subtilis)

Our adviceFor cleaning the external partsof your generator, use SURFA’SAFEPREMIUM (p.12)

AUTOMATIC DILUTIONActive from 15 min.


LAUNDRY TREATMENT

PACKAGING - REF4 cans, 5L each .....................................1609.03725L can .................................................1609.018

PACKAGING - REF4 cans, 5L each .....................................203.037


BIOCIDAL PRODUCTS REGULATION (EU) 528/2012

DefinitionThe aim of biocidal products is to destroy, fight off or render inoffensive harmful organisms, prevent their action or fight them in any other manner, by an action other than a simple physical or mechanical one. This applies to any active substances and to products containing or generating one or more active substances.

ObjectiveThe Biocidal Products Regulation has the same objectives as the Biocidal Products Directive that it replaces. It is based on a desire, at European le-vel, to control the effectiveness of biocidal products, while respecting hu-man and animal health and the environment. It will result in a Marketing Authorization for biocidal products at national or Community level after evaluation of their effectiveness and the risks from their use. This can only occur after authorization of active biocidal substances at Commu-nity level, and also after their evaluation in terms of benefits and risks.

4 groups of biocidal products» Group 1: Disinfectants This group includes 5 Types of Product (TP):- TP 1: Biocidal products for human hygiene.This does not concern:- antiseptic products for the skin that can be applied to injured skin or skin that may be injured (these comply with the requirements of regula-tions relating to pharmaceuticals);- cosmetics: body hygiene and skincare products (these comply with the cosmetics regulation);- TP 2: Disinfectants and algicides not intended for direct application on human beings or animals.Specifically:- products used to disinfect surfaces, materials, foodstuffs or animal feed;- products used to disinfect the air, water not used for human or animal consumption, chemical toilets, wastewater, hospital waste and soil.This does not concern:Products intended specifically for the disinfection of medical devices. These fall under the regulations concerning medical devices. - TP 3: Biocidal products for veterinary hygiene.- TP 4: Disinfectants for surfaces in contact with foodstuffs and animal feed.- TP 5: Disinfectants for potable water.

» Group 2: Protection products: wood protection, detergent preservatives, etc. (TP 6 to 13).

» Group 3: Products for pest control: repellents, insecticides, etc. (TP 14 to 20).

» Group 4: Other biocidal products: stain-repellents, embalming and taxidermy products (TP 21 and 22).

ImplementationThe evaluation of substances is currently in progress and a new imple-mentation schedule up to 2024 has been established by the European Chemicals Agency (ECHA) for completion of the review of all biocidal substances.This new deadline does not change the obligations that are already ap-plicable, especially in terms of formulation (use of active biocides under examination) and labeling. As regards disinfecting biocidal substances, the evaluation schedule is going ahead, with approvals expected to be issued in the next 5 years. The marketing authorization application folders for disinfectant products containing them will have to be submitted within one and a half to two years after the date of approval of the active substance.

» As a user, is this regulation of any concern to me?Besides the obligations that are applicable to the manu-facturers of biocidal substances and the formulators that use these substances, the biocidal products regulation also includes obligations for the users of the said biocidal products.

» TodayOnly the use of disinfectant biocidal products with notified active substances in course of evaluation for adequate usage is possible. This can be controlled at the user’s pre-mises, specifically by the DRIRE (Regional Directorates for Industry, Research and the Environment).

» TomorrowAfter the end of the transition period, users will be obliged to use products with MAs (Marketing Authorizations).It will be the user’s responsibility to ensure that the ins-tructions for use and the conditions of usage (dilution - contact times - temperature) contained in previously validated protocols, are consistent with the conditions of the product’s MA.Every application of a biocidal product must be included in the strict conditions of the MA.

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STANDARDS

STANDARDS GLOSSARY

EN 1040 : Staphylococcus aureus – Pseudomonas aeruginosaBasic bactericidal activity –Phase 1. Suspension test in 5 minutes (or 1, 15, 30 and 60 minutes), at +20°C (or others within +4°C, +10°C, +40°C) –Microbial reduction ≥105 (5 log).

EN 13727+A1 (December 2013) : Staphylococcus aureus – Pseudomonasaeruginosa – Enterococcus hirae - Escherichia coli (only for hands)Bactericidal activity – Phase 2/Step 1 - Medical. Quantitative suspension test. *Hygienic rubbing and handwash: 30 to 60 sec maximum, at +20°C, dilution in hard water 30°f, in the presence of interfering substances (Hygienic rubbing: CC: 0.3 g/L albumin ; hygienic handwash: DC: 3 g/L albumin + 3 ml/L erythrocytes; or others) - Microbial reduction ≥105 (5 log) - Microbial reduction ≥103 (3 log) for hygienic handwash..*Surgical rubbing and handwash: 1 to 5 min maximum, at +20°C, dilution in hard water 30°f, in the presence of interfering substances (Surgical rubbing: CC: 0.3 g/L albumin ; Surgical handwash: DC: 3 g/L albumin + 3 ml/L erythrocytes; or others) - Microbial reduction ≥105 (5 log).* Instruments: Time according to the manufacturer, 60 min maximum, from +20°C to +70°C, dilution in hard water 30°f, in the presence of interfering substances (CC : 0,3 g/L albumin; DC : 3 g/L albumin + 3 ml/L erythrocytes; or others) - Microbial reduction ≥105 (5 log).* Surfaces : Time according to the manufacturer, from 5 to 60 min maximum, from +4°C to +30°C, dilution in hard water 30°f, in the presence of interfering subs-tances (CC : 0,3 g/L albumin; DC : 3 g/L albumin + 3 ml/L erythrocytes; or others) - Microbial reduction ≥105 (5 log).

EN 1276 : Staphylococcus aureus – Pseudomonas aeruginosa – Enterococcus hirae – Escherichia coliBactericidal activity – Phase 2/Step 1 - Industry. Domestic. Communities. Quantitative suspension test in 5 minutes (or other additional), at +20°C (or +4°C, +10°C, +30°C ou +40°C), dilution in hard water 30°f, in the presence of interfering substances (CC: 0.3 g/L albumin; DC: 3 g/L albumin; or others) - Microbial reduction ≥ 105 (5 log).

EN 14561 : Staphylococcus aureus – Pseudomonas aeruginosa – Enterococcus hiraeBactericidal activity – Phase 2/Step 2 - Medical. Quantitative carrier test by im-mersion in 60 minutes (or 5, 15 and 30 minutes), at +20°C (or others with 10°C interval, 60°C maximum), dilution in hard water 30°f, in the presence of interfering substances (CC: 0.3 g/L albumin + 30°f hard water; DC: 3 g/L albumin + 3 ml/L erythrocytes + 30°f hard water; or others) - Microbial reduction ≥ 105 (5 log).

EN 13697 : Staphylococcus aureus – Pseudomonas aeruginosa – Enterococcus hirae – Escherichia coliBactericidal activity – Phase 2/Step 2 - Industry. Domestic. Communities. Sur-faces. Quantitative carrier test in 5 minutes (or 1, 15, 30 and 60 minutes), at +20°C (or +4°C, +10°C and +40°C), dilution in hard water 30°f, in the presence of interfering substances (CC: 0.3 g/L albumin; DC: 3 g/L albumin; or others) - Microbial reduction ≥ 104 (4 log).

EN 14348 : Mycobacterium terrae – Mycobacterium aviumMycobactericidal / tuberculocidal activity – Phase 2 / Step 1 - Medical. Instru-ments. Quantitative suspension test in 60 minutes (or 5, 15 and 30 minutes) at +20°C (or others with 10°C interval), dilution in hard wtare 30°f, in the presence of interfering substances (CC: 0.3 g/L albumin; DC: 3 g/L albumin + 3 ml/L erythro-cytes; or others) – Microbial reduction ≥ 104 (4log).

EN 14563 : Mycobacterium terrae – Mycobacterium aviumMycobactericidal / tuberculocidal activity – Phase 2 / Step 2 - Medical. Ins-truments. Quantitative carrier test by immersion in 60 minutes (or 5, 15 and 30 minutes) at +20°C (or others with 10°C interval, +60°C maximum), dilution in hard water 30°f, in the presence of interfering substances (CC: 0.3 g/L albumin; DC: 3 g/L albumin + 3 ml/L erythrocytes; or others) – Microbial reduction ≥ 104 (4 log).

EN 1275 : Candida albicans – Aspergillus nigerBasic fungicidal/yeasticidal activity – Phase 1. Suspension test in15 minutes (or 1, 5, 30 and 60 minutes), at +20°C (or others +4°C, +10°C, +40°C) – Microbial reduction ≥ 104 (4 log).

EN 13624 (September 2013) : Candida albicans – Aspergillus brassiliensisFungicidal/yeasticidal activity – Phase 2/Step 1 - Medical. Instruments. *Hygienic rubbing and handwash: test on Candida albicans from 30 to 60 sec maximum at +20°C, dilution in hard water 30°f, in the presence of interfe-ring substances (Hygienic rubbing: CC: 0.3 g/L albumin ; Hygienic handwash: DC: 3 g/L albumin + 3 ml/L erythrocytes ; or others) - Microbial reduction ≥ 104 (4 log) - Microbial reduction ≥ 102 (2 log) for hygienic handwash. *Surgical rubbing and handwash: test on Candida albicans from 1 to 5 min maximum at +20°C, dilution in hard water 30°f, in the presence of interfe-ring substances (Surgical rubbing: CC: 0.3 g/L albumin ; Surgical handwash: DC: 3 g/L albumin + 3 ml/L erythrocytes ; or others) - Microbial reduction ≥ 104 (4 log). *Instruments: Time according to the manufacturer, 60 min maximum, from +20°C to +70°C, dilution in hard water 30°f, in the presence of interfering subs-tances (CC : 0,3 g/L albumin; DC : 3 g/L albumin + 3 ml/L erythrocytes; or others) - Microbial reduction ≥104 (4 log).* Surfaces: Time according to the manufacturer, from 5 to 60 min maximum, from +4°C to +30°C, dilution in hard water 30°f, in the presence of interfering subs-tances (CC : 0,3 g/L albumin; DC : 3 g/L albumin + 3 ml/L erythrocytes; or others) - Microbial reduction ≥104 (4 log).

EN 1650+A1 (July 2013) : Candida albicans – Aspergillus brassiliensis Fungicidal/yeasticidal activity – Phase 2/Step 1 - Industry. Domestic. Communi-ties. Quantitative suspension test in 15 minutes (or 1, 5, 30 and 60 minutes), at +20°C (or +4°C, +10°C and +40°C), in the presence of interfering substances (CC: 0.3 g/L albumin + 30°f hard water; DC: 3 g/L albumin + 30°f hard water; or others) – Microbial reduction ≥ 104 (4 log).

EN 14562 : Candida albicans – Aspergillus nigerFungicidal/yeasticidal activity – Phase 2/Step 2 - Medical. Instruments. Quan-titative carrier test by immersion in 60 minutes (or 5, 15 and 30 minutes), at +20°C (or others with 10°C interval, maximum of 60°C), in the presence of inter-fering substances (CC: 0.3 g/L albumin + 30°f hard water; DC: 3 g/L albumin + 3 ml/L erythrocytes + 30°f hard water; or others) - Microbial reduction ≥104 (4 log).

EN 13697 : Candida albicans – Aspergillus nigerFungicidal/yeasticidal activity – Phase 2/Step 2 - Industry. Domestic. Communi-ties.Surfaces. Quantitative carrier test in 15 minutes (or 1, 5, 30 and 60 minutes), at +20°C (or +40°C, +10°C and +40°C), in the presence of interfering subs-tances (CC: 0.3 g/L albumin + 30°f hard water; DC: 3 g/L albumin + 30°f hard water; or others) - Microbial reduction ≥103 (3 log).

EN 14476 (September 2013) : Poliovirus – Adenovirus – Norovirus murin - Par-vovirus (only for instruments with a t° > 40°C and for textiles)Virucidal activity – Phase 2/Step 1 - Medical. Quantitative suspension test.*Hands: Time according to the manufacturer, from 30 sec to 3 min maximum, at +20°C, dilution in hard water 30°f, in the presence of interfering substances (CC : 0,3 g/L albumin; DC : 3 g/L albumin + 3 ml/L erythrocytes; or others) - Microbial reduction ≥104 (4 log).*Instruments: Time according to the manufacturer, 60 min maximum, from +20°C to +70°C, dilution in hard water 30°f, in the presence of interfering subs-tances (CC : 0,3 g/L albumin; DC : 3 g/L albumin + 3 ml/L erythrocytes; or others) - Microbial reduction ≥104 (4 log).* Surfaces: Time according to the manufacturer, from 5 to 60 min maximum, from +4°C to +30°C, dilution in hard water 30°f, in the presence of interfering subs-tances (CC : 0,3 g/L albumin; DC : 3 g/L albumin + 3 ml/L erythrocytes; or others) - Microbial reduction ≥104 (4 log).* Surfaces: Time according to the manufacturer, 20 min maximum, from +30°C to +70°C, dilution in hard water 30°f, in the presence of interfering substances (CC : 0,3 g/L albumin; DC : 3 g/L albumin + 3 ml/L erythrocytes; or others) - Microbial reduction ≥104 (4 log).

64

STANDARDS

STANDARDS GLOSSARY

Activity on virusesAdaptation of the EN 14476 standard for HIV-1, PRV (surrogate of HBV), BVDV (surrogate of HCV), Herpesvirus, Rotavirus, Norovirus, Coronavirus (SARS), In-fluenza virus A H1N1, Vaccinia virus… Viral reduction≥104 (4 log).

EN 13704 : Bacillus subtilisSporicidal activity – Phase 2/Step 1 - Industry. Domestic. Communities. Surfaces. NEP. Quantitative suspension test in 60 minutes (or 5, 15 and 30 minutes), at +20°C (or +40°C, +10°C, +40°C and +75°C), dilution in hard water +30°f, in the presence of interfering substances (CC: 0.3 g/L albumin) - Microbial reduction ≥103 (3 log).

EN 1499 (June 2013)Hygienic Handwash – Phase 2/Step 2. Test on voluntaries with handsartificially contaminated with Escherichia coli K12, in the practical conditions of use, in 30 or 60 seconds. The reduction factor obtained is compared to those obtained in the same conditions with a standard washing (CODEX plain soap).

EN 1500 (June 2013)Hygienic Hand rubbing – Phase 2/Step 2. Test on voluntaries with handsartificially contaminated with Escherichia coli K12, in the practical conditions of use, in 30 or 60 seconds. The reduction factor obtained is compared to those obtained in the same conditions with a standard washing (60% propanol-2).

EN 12791Surgical disinfection of hands – Phase 2/Step 2. Test on natural flora ofvoluntaries. Assesment of the immediate effect and 3 hours after disinfection. The reduction factor obtained is compared to those obtained in the same conditions with a standard washing (60% propanol-2).

EN 14347 : Bacillus subtilis – Bacillus cereusBasic sporicidal activity - Phase 1. Quantitative suspension test in 30, 60 or 120 min, at +20°C - Microbial reduction ≥104 (4 log).

NF T 72-281Airborne disinfection of surfaces - Determination of bactericidal and/or fungicidal and/or sporicidal activity. – Microbial reduction ≥105 bacteria (5 log) ; ≥104 yeasts/moulds (4 log) ; ≥103 spores of bacteria (3 log).

NF T 72-230/231Sporicidal activity – Quantitative suspension test in 60 minutes at +20°C– Microbial reduction ≥105 (5 log).

EN 13623 Legionella pneumophilaBactericidal activity - Phase 2 / step 1 - Quantitative suspension testin 60 mi-nutes (or others, at +20°C or +30°C, dilution in hard water 30°f, in the presence of interfering substances (0,05% yeast extract) - Microbial reduction ≥104 (4 log).

EN 13610Virucidal activity - Phase 2 / Step 1 - Industry. Domestic. Communities. Quanti-tative suspension test in 15 minutes (or 5, 30 and 60 min), at +20°C (or +4°C, +10°C and +40°C), dilution in hard water 30°f and in the presence of interfering substances (1% milk serum; or 1% skimmed milk) - Microbial reduction ≥104 (4 log).

Antimicrobial preservation efficacyEuropean Materia Medica method. Determination of a preservative’s antimicrobial activity.

EN ISO 11931Evaluation of the antimicrobial protection of a cosmetic product.

MEDICAL COMMUNITIES

BASIC STANDARDSPHASE 1

Suspension tests to determine basis activity

EN 1040 : bactericidal activity

EN 1275 : fungicidal and/or yeasticidal activity

EN 14347 : sporicidal activity

STANDARDS OF APPLICATION HANDS INSTRUMENTS SURFACES

PHASE 2 STEP 1

Suspension tests in the representative practical conditions of use

EN 13727 : bactericidal activity EN 1276 : bactericidal activity

EN 14348 : mycobactericidal and/or tuberculocidal activity

EN 13624 : fungicidal and/or yeasticidal activityEN 1650 : fungicidal and/or

yeasticidal activity

EN 14476 : virucidal activity EN 13610 : virucidal activity

PHASE 2 STEP 2

Tests simulating the practical conditions of use (carrier tests, handwash or hand-rub tests)

EN 1499 : Hygienic handwashEN 1500 : Hygienic hand rubbingEN 12791 : Surgical disinfection

EN 14561 : bactericidal activity EN 13697 : bactericidal activity

EN 14563 : mycobactericidal and/or tuberculocidal activity



EUROPEAN STANDARDS OF ANTIMICROBIAL EFFICACY

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Pavé du Moulin - 59260 Lille-Hellemmes FRANCETél. +33 3 20 67 67 67 - Fax. +33 3 20 05 27 48www.anios.com

Fully commited to the fight against Nosocomial Infections since 1898

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A collaboration with W.H.O. Private Organizations for Patient Safety

Simple operation

All-day ready for use

Increased sealing speed

Constant sealing pressure

Digital temperature control

Sealing technique according to DIN 58953, PART 7

Safety tested and approved by EN, VDE

Built-in cooling control

Practical worktop available as optional extra

Shock watch system for delivery safety

Rotosealer RS-120Economical choice for smallclinics

Wipak OyP.O. Box 45, Wipaktie 2

FI-15561 Nastola, FinlandTel. +358 (0)20 510 311Fax +358 (0)20 510 3333

E-mail: [email protected] www.wipak.com

Rotosealer RS-120continually ready for use for quick and reliable closingof all heat-sealable materials.

• M

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Safe and quick sealing process

• Sealing temperature is easily adjustable to suit the material being sealed.

• When switched on, the motor and conveyor belts start automatically.

• The package is conveniently carried by the conveyor belts through the

heating and sealing rollers to achieve quick and efficient closure.

• Adjustable in-feed guiding plate provides predefinition of the seal distance

(0 - 35mm) from the package edge.

• Built-in fan improves the inside temperature control and minimizes

overheating risk in all-day use.

The package is hermetically sealed toprotect against bacteria.

The Steriking® Rotosealers providea strong seal. Total seal width is 12 mm.

The white epoxy coated housing iseasy to maintain and to keep clean.

N/m

EN

mm12

SEA

L ST

REN

GTH

SEAL STRUCTURE

100

Warranty

Shock watch label

Seal width 12 mmSealing speed 10 m/minSealing temperature 0 - 220 °CTemp. tolerance ±2 %Power consumption 250 W (max 600 W)Power supply 220/240 V 50/60HzWeight 15 kgDimensions 490 x 255 x 160 mmSeparate worktop 625 x 225 x 60 mm

• 24 months from the date of purchase.

• Enables recognition of transport damage.• Adhered to the transport carton.

Detailed operating manual and list of spare parts come with each unit.

Technical data

3M Sterilization Assurance Full Line CatalogComplete sterilization assurance products

39390 catalog 3.qxd 4/12/02 4:13 PM Page A

Record Keeping 28Record Keeping Software 29Log Books, Envelopes and Record Charts 29 Load Record Cards 30Sterilization Integrator Load Record Card 30Label Gun System 31

Cleaning and Decontamination 32Multi-Enzyme Detergent 33

Sterilization Hardware 34Gas Sterilizers/Aerators 35Aerator 363M™ EtO-Abator System 36Drying Cabinet 37Transfer Cart 37Ethylene Oxide (EO) Gas Cartridges 38Printer Paper 38Packaging 39Ethylene Oxide (EO) Monitoring Badge 39

Index35 40

ContentsIntroduction 2

Biological Indicators 6Rapid Readout Biological Indicators and Test Packs 7Auto-readers 8Biological Indicators and Test Packs 9Biological Indicator Monitoring Starter Kit 10Biological Indicator Incubators 10

Enzymatic Indicators 11Enzymatic Indicators and Challenge Packs 12

Chemical Indicators 13Steam and Ethylene Oxide (EO) Chemical Integrator Test Pack 14Steam Chemical Integrators 15Steam Chemical Indicator-Plus Strips 15Steam Chemical Indicator Strips 16Chemical Indicator Roll–Steam 16Low Temperature Chemical Indicators 17–18Chemical Indicator Roll–Ethylene Oxide (EO) 18Dry Heat Chemical Indicators 19Glutaraldehyde Monitors 20Instrument Protectors 21Sterilization Indicator Labels 21

Bowie-Dick Test Pack and Sheets 22Bowie-Dick Plus Test Pack with Early Warning Test Sheet 23Bowie-Dick Type Test Pack and Sheets 23

Indicator Tapes 24Indicator Tape for Steam Sterilization 25Steam Indicator Tape for Disposable Wraps 26Indicator Tape for Ethylene Oxide (EO) Sterilization 26Indicator Tape Dispensers 27

39390 catalog 3.qxd 4/12/02 4:13 PM Page B

32

3M Sterilization Assurance

Introduction

Providing a full line of options for sterilization process monitoring.

In today’s economic climate, with tighter health care budgets, the prevention of infection is critical to curbing

the enormous costs associated with surgical site infections. What you do every day as a sterilization health care

professional can help reduce the risk of costly infections.

To determine the effectiveness of the entire sterilization process, 3M provides a complete quality sterilization

monitoring program consisting of five basic steps: Load Control, Pack Control, Equipment Control, Exposure

Control and Record Keeping.

We invite you to look into this comprehensive sterilization monitoring program from the industry leader.

3M has been in the sterilization monitoring industry for more than 40 years. With pioneering efforts in the

development of sterilizers, indicator tapes, and self-contained biological indicators, this comprehensive program

provides time-tested accuracy for sterilization assurance in all areas of monitoring from load control to record

keeping, and has become a model for all other sterilization monitoring systems to follow.

You can’t afford the risk of an undetected sterilization process failure. We’re here to work with you to re-evaluate

products, processes and policies throughout your organization.

Working directly with you.

3M understands the challenges you’re facing in sterilization. Growing concerns about risk management and

health care liability, shrinking budgets and stringent documentation requirements. The need to standardize

policies and procedures for a variety of health care settings and locations.

We’ll work with you to meet the varying needs of your organization...from the high volume of large facilities

to the individualized needs of outpatient surgery centers and primary care clinics.

In today’s health care environment, you need accuracy, credibility and efficiency in all phases of the

sterilization process. 3M stands ready to put our leadership, products and services to work for you.

As a worldwide leader in sterilization assurance, 3M’s comprehensive product line is backed by excellence

in innovation, experience and service.

Steps in the sterilization process.

Sterilization is performed to minimize the risk of surgical site infection by destroying all forms of microorganisms

including bacteria, viruses, spores and fungi on an object. The goal of the sterilization process is to assure that

all surgical instruments are free from contamination before surgery. This helps improve patient outcomes and

protects patients from harm. There are five basic steps in the sterilization process itself: Clean, Prep/Pack, Sterilize,

Store and Issue/Use.

Clean and DecontaminateThe presence of soil or organic material on instruments can reduce disinfection or sterilization effectiveness byencapsulating microorganisms and preventing penetration of the disinfectant or sterilant. In addition, the presence oforganic soil can inactivate some disinfectants. The firststep in the sterilization process, clean and decontaminate,addresses the removal of foreign material and makesinstruments ready for further processing.

Prep and PackPrep and Pack is the next step in the five basic steps of the sterilization process. The effectiveness of thesterilization process depends upon the type of packagingmaterial used and the procedure used for prepping,packaging and loading the items to be sterilized. The proper selection of packaging material and the use of internal and external chemical indicators will help customers identify the effectiveness of this step in the process.

SterilizeIn the third step of the sterilization process, instrumentsare exposed to the actual sterilant (steam, ethylene oxide,etc.) or high level disinfectant (glutaraldehyde, etc.) A check of the sterilizer/processor is required to ensurethat it is functioning properly and that the correct qualityand quantity of sterilant or high level disinfectant is usedand that the correct cycle parameters were chosen. This is done through the use of readings and printouts from the equipment and the proper selection and use ofbiological, enzymatic and chemical indicators.

StoreFirst, instruments are removed from the sterilizer/processor and record documentation is completed. Then, appropriate storage is required to maintain the

integrity of the packaging and level of sterility of theinstrument(s) prior to use. Documentation for eachindividual pack is recommended by AAMI, ASHCSP, AORN and JCAHO to ensure that a load or pack can be identified and found in the event of a recall. Thisdocumentation is part of a total record keeping system.

Issue and UseWhen items are requested for use they are retrieved from storage and checked to ensure that the external pack monitor has reached its endpoint (eg. color change)and then issued for use. At the point of use, internal packmonitors are checked to ensure that sterilization processconditions penetrated to the inside of the pack. Next, the instruments are used and then sent back for cleaningand decontamination.

3M Sterilization Assurance Program

39390 catalog 3.qxd 4/12/02 4:13 PM Page 2

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3M Sterilization Education Programs

Continuing education has become increasingly important in many professions and nowhere is it more

critical than in the health care arena. With increasing demands on limited resources, access to educational

programs is often reduced or restricted. 3M Health Care has a long-standing tradition of commitment to

education and we are proud to be able to offer you a full education continuum.

We recognize that people are individuals with different learning styles and abilities. With this in mind,

we have put together a comprehensive range of educational opportunities from which you may select;

those that are appropriate to the individuals within your unit. If you would like further details of any

of these programs, please contact the 3M Health Care Customer Helpline at 1-800-228-3957.

The following is a sample of the full range of 3M’s educational programs and materials for the infection

control, operating room and central supply personnel within your facility.

Examples of 3M Sterilization Assurance Educational Programs and Materials

Sterilization Issues Covering the latest developments in infection control and sterilization.and Answers Course

Infection Control Rounds An educational publication featuring articles on infection control and sterilization.

3M Sterilization Helping meet local educational objectives by organizing speakers Speaker Program for specialized program topics.

In-Service Videos An extensive video library, making in-service training easier for your organization.

Interactive Education CD-ROM programs that facilitate training on best practice guidelines for infection prevention.

Purdue/IAHCSMM A bimonthly educational publication in Health Care Purchasing News trade journal and IAHCSMM newsletters, sponsored by 3M.

3M Sterilization Assurance Program continued

An undetected sterilization process failure can put patients, staff and the financial health of your facility at risk.

Additional costs associated with postoperative infections, and other health care liabilities, make the implementation

of a sterilization process monitoring program an extremely critical practice for all health care facilities. The 3M

Sterilization Assurance Program is a comprehensive and practical approach to sterilization monitoring procedures

and methods that you can count on to reduce your risk of an undetected sterilization process failure.

The 3M Sterilization Assurance Program is the most comprehensive sterilization monitoring system ever developed.

And because the products are designed to monitor the sterilizer, as well as every load and every pack, the 3M

Sterilization Assurance Program provides a high level of confidence that sterile conditions have been met. The days

of waiting for an accurate sterilization reading are gone.

The 3M Sterilization Assurance Program offers:

Rapid Release of Critical DevicesA series of checks and balances makes it possible to verify if conditions for sterilization of implantableshave been achieved.

Elimination of RecallsBecause the 3M Sterilization Assurance Program monitors the sterilizer as well as each pack, you’ll know if conditions for sterilization have been met and the load can be released from sterile processing.

Less Purchasing of InstrumentsYou can manage your current inventory more efficiently,potentially saving your health care facility a substantialamount of money.

Reduction in the Risk of InfectionNonsterile instruments and implantables are a probablecause of surgical wound infections. The 3M SterilizationAssurance Program signals your staff immediately to sterilization process problems that could lead tononsterile medical devices.

Reduction and Control of Sterilizer DowntimeYou can be alerted to problems before they becomeserious—enabling you to schedule service at a timethat’s convenient.

Documentation to Help Meet Accreditation RequirementsThe 3M Sterilization Assurance Program record keeping system enables you to record and store all sterilization data in an easily retrievable format and meet recommended standards and practices.


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Issue/UseStoreSterilizePrep/PackClean/Decontaminate

Load ControlThe sterilization reliability that only a biological indicator can deliver

Biological Indicators

• Results in one hour (1291) or three hours (1292)

• Test packs present a challenge to the sterilization process as do the AAMIrecommended packs

• Make decisions and take appropriate action before surgery

• Every load monitoring and quarantining can eliminate recalls

• The Attest rapid readout biological monitoring system can help reduce the costs associated with fighting infections—a cost measured in both dollars and time spent

• Malfunctioning sterilizers can be repaired and put back into service quickly

3M™ Attest™ Rapid Readout Biological Indicator for 270°F/132°C Gravity Displacement Steam Sterilizers

Cat. # Description Packaging Shipping

1291* Steam Biological Indicator 50 each/box 4 boxes/case

3M™ Attest™ Rapid Readout Biological Indicators for 250°F/121°C Gravity and 270°F/132°C Vacuum-Assisted Steam Sterilizers


1292* Steam Biological Indicator 50 each/box 4 boxes/case

1296* Steam Biological Test Pack (25 controls) 25 packs/box 1 box/case

1296F* Steam Biological Test Pack (5 controls) 25 packs/box 1 box/case

*Must be used in conjunction with 3M™ Attest™ Model 190 or 290 Auto-reader

Rapid Readout Biological Indicators and Test Packs

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Biological Indicators and Test Packs

• Biological indicator vials are easy to use and interpret with visual colorreadout in 24 hours (1261) or 48 hours (1262/1264)

• Test packs present a challenge to the sterilization process as do the AAMIrecommended test packs

• Each test pack contains an Attest 1262 or 1264 biological indicator

3M™ Attest™ Biological Indicators for 270°F/132°C Gravity Displacement Steam Sterilizers


1261 Steam Biological Indicator 100 each/box 4 boxes/case

1261P Steam Biological Indicator 25 each/box 4 boxes/case

3M™ Attest™ Biological Indicators for 250°F/121°C Gravity and 270°F/132°C Vacuum-Assisted Steam Sterilizers


1262 Steam Biological Indicator 100 each/box 4 boxes/case

1262P Steam Biological Indicator 25 each/box 4 boxes/case

1276 Steam Biological Test Pack 25 each/box 1 box/case(25 controls/box)

1276F Steam Biological Test Pack 25 each/box 1 box/case(5 controls/box)

3M™ Attest™ Steam-Plus Test Pack

Each pack consists of an Attest 1262 Biological Indicator and a 3M™ Comply™ (SteriGage™)Steam Chemical Integrator. For use in every load.


41380 Steam-Plus Test Pack 16 each/box 4 boxes/case(4 controls/box)

3M™ Attest™ Biological Indicators for Ethylene Oxide (EO)


1264 Ethylene Oxide (EO) Biological Indicator 100 each/box 4 boxes/case

1264P Ethylene Oxide (EO) Biological Indicator 25 each/box 4 boxes/case

1278 EO Test Pack (25 controls) 25 each/box 2 boxes/case

1278F EO Test Pack (5 controls) 25 each/box 2 boxes/case

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• 14-vial capacity, 60˚C steam incubation temperature

• Built-in fluorescent reader with manual calibration and readout in 1 or 3 hours

• For use with 3M™ Attest™ Rapid Readout Biological Indicators

3M™ Attest™ 190 Auto-reader


190* 120V nominal voltage required; 108-132V 1 unit/box 1 box/caseacceptable voltage range

78-8078-7349-8 UV Bulb and Starter Kit (only sold direct) - 1 each/case

*Only available from your 3M sales representative.

• The Attest 290 auto-reader does not require time-consuming calibration

• Audible alarm sounds for improved monitoring

• Does not require any routine maintenance

• For use with 3M™ Attest™ Rapid Readout Biological Indicators

3M™ Attest™ 290 Auto-reader


290* 120V nominal voltage required; 108-132V 1 unit/box 1 box/caseacceptable voltage range

78-2007-2981-5 Power cord for Attest 290 auto-reader 1 ea/case

*Only available from your 3M sales representative.

Auto-readers


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Enzymatic Indicators



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FPOneed family shot or ps label

Everything you need for effective monitoring of the steam sterilization process.

3M™ Attest™ Biological Indicator Monitoring Starter Kit

Consists of one roll of 3M™ Comply™ 1222-6N Indicator Tape, one box of 3M™

Attest™ 1262P Biological Indicators, one 3M™ Attest™ 116 Incubator, one bag of 3M™ Comply™ 1243B Chemical Integrators, one 3M™ 1266 Log Book,in-service video and wall chart.


115 3M Attest Monitoring Kit 1 each/box 1 box/case

A full line of Attest incubators provide optimal conditions for accurate readout of Attest biological indicators.

• Convenient, 14- or 28-vial capacity

• Dry-block design pre-set to proper incubation temperature

3M™ Attest™ Biological Indicator Incubators


116 14-vial (round); 56˚C (Steam); 120 nominal voltage required; 1 each/box 1 box/case90–132V acceptable

117 14-vial (round); 37˚C (EO); 120 nominal voltage required; 1 each/box 1 box/case90–132V acceptable

126 28-vial (2-tier); 56˚C (Steam); 120 nominal voltage required; 1 each/box 1 box/case90–132V acceptable

127 28-vial (2-tier); 37˚C (EO); 120 nominal voltage required; 1 each/box 1 box/case90–132V acceptable

130 28-vial (2-tier); 37˚C/56˚C (EO & Steam); 120 nominal 1 each/box 1 box/casevoltage required; 90–132V acceptable

Biological Indicator Monitoring Starter Kit

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Biological Indicator Incubators

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Enzymatic Indicators and Challenge Packs

These indicators and challenge packs are used to monitor steam sterilization cycles.

• Requires no incubation and no other instrumentation to interpret results

• Easy-to-read results in 20 seconds

• Reusable challenge pack (use up to 20 times)

3M™ Rapid Enzymatic Indicators for 250˚F/121˚ Displacement and 273˚/134˚ Vacuum Assisted Gravity Steam Sterilization


2482 Enzymatic Indicator 100 test units, indicator 1 box/casesolution/box

2482F Enzymatic Indicator 50 test units, 1 box/caseindicator solution/box

2482T Enzymatic Indicator 10 test units, 1 box/caseindicator solution/box

3M™ Rapid Enzymatic Indicators and Challenge Packs for 273˚/134˚ Vacuum Assisted Steam Sterilization


2486 Enzymatic Indicator 4 challenge packs, 100 test units, 1 box/caseand Challenge Packs indicator solution/box

2486F Enzymatic Indicator 2 challenge packs, 50 test units 1 box/caseand Challenge Packs indicator solution/box

2483 Challenge Packs 5 challenge packs/box 1 box/case

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Chemical Indicators




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3M Comply chemical integrators offer an immediate, accurate and easy-to-readmethod of monitoring sterilization process conditions inside each pack.

• Available for steam sterilization cycles

• “Moving front” style has accept/reject readout for instant results withoutinterpretation, convenient small size for all packs, and optional extendersavailable for easy retrieval from inner packs

• Immediately identify problems in specific packs

• Safe, non-toxic chemicals; no worry of contamination or transfer to sterile items

3M™ Comply™ (SteriGage™) Steam Chemical Integrators


1243A Steam Chemical Integrator; moving front; 500 each/bag 2 bags/case2 in. x 3/4 in. (5,1 cm x 1,9 cm)

1243B Steam Chemical Integrator; moving front; 100 each/bag 10 bags/case2 in. x 3/4 in. (5,1 cm x 1,9 cm)

1243E Steam Chemical Integrator; moving front with extender; 1000 each/bag 1 bag/case9 in. x 3/8 in. (22,9 cm x 1,0 cm)

1240E Extender only; 2500 each/bag 2 bags/case7-1/2 in. x 3/8 in. (19,1 cm x 1,0 cm)

Steam Chemical Integrators

Steam Chemical Indicator-Plus Strips

Each strip has two purple ink bars that are sterilantspecific and change color in sequence during exposureto saturated steam. A clear protective coating over theink bars prevents the ink from touching items beingsterilized.

3M™ Comply™ Steam Chemical Indicator-Plus Strips


00117 Short Form—270˚F Indicator 200 each/box 20 boxes/case5/8 in. x 4-1/4 in. (1,5 cm x 10,8 cm) for use in 270˚F vacuum-assisted and gravity sterilizers

00118 Long Form—270˚F Indicator 5/8 in. x 7-3/8 in.; 200 each/box 20 boxes/case5/8 in. x 7-3/8 in. (1,5 cm x 18,7 cm)for use in 270˚F vacuum-assisted and gravity sterilizers

00119 250˚F Indicator, 5/8 in. x 4-1/4 in.; 200 each/box 20 boxes/case5/8 in. x 4-1/4 in. (1,5 cm x 10,8 cm)for use in 250˚F gravity sterilizers

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Steam Chemical Integrator Test Pack

Pack consists of a 3M™ Comply™ (SteriGage™) Steam Chemical Integrator in a small test pack of porous substrate with a moisture impervious, quality CSR wrap.


3M™ Comply™ (SteriGage™) Steam Chemical Integrator Test Pack


41360 Pack with Comply (SteriGage) Steam 16 packs/box 4 boxes/caseChemical Integrator

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EO Chemical Integrator Test Pack

Pack consists of a 3M™ Comply™ (SteriGage™) EO Chemical Integrator inside aprecisely engineered pack. For use in every load of EO/HCFC gas mixtures inconjunction with a biological indicator test pack.


3M™ Comply™ (SteriGage™) EO Chemical Integrator Test Pack


45260 Pack with Comply (SteriGage) 16 packs/box 4 boxes/caseEO Chemical Integrator

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Single use chemical indicator for use in the Steris® System 1 processor. Indicator provides assurance that items have been exposed to the appropriateconcentration of sterilant. Indicator changes from red (unprocessed) to green(processed) color for easy interpretation. Large size and distinct color for easyretrieval of the indicator from processor.

3M™ Comply™ Liquid Peracetic Acid Chemical Indicator


1249 Comply Liquid Peracetic Acid Chemical Indicator 50 items/pouch 4 pouches/case1-3/4 in. x 1-3/4 in. (4,4 cm x 4,4 cm)

An internal pack chemical indicator for use in STERRAD® SterilizationProcesses (models 100, 100S and 50). The indicator provides assurance thatitems inside a pack have been exposed to sterilant. Indicator changes from blueto pink when exposed to vapor hydrogen peroxide. Indicator color does not fadewhen exposed to light.

3M™ Comply™ Gas Plasma Chemical Indicator Strip


1248 Comply Gas Plasma Chemical Indicator Strip 250 each/box 4 boxes/caseStrip; 13/16 in. x 4 in. (2,0 cm x 10 cm)

3M™ Comply™ Chemical Integrators offer an immediate, accurate and easy-to-read method of monitoring sterilization process conditions inside each pack.

• Available for EO/HCFC gas mixture sterilization cycles.

• “Moving front” style has accept/reject readout for instant results withoutinterpretation, convenient small size for all packs, and optional extendersavailable for easy retrieval from inner packs.

• Immediately identify problems in specific packs.

• Safe, non-toxic chemicals; no worry of contamination or transfer to sterile items.

3M™ Comply™ (SteriGage™) EO Chemical Integrators


1244A EO Chemical Integrator; moving front; for gas 500 each/bag 2 bags/casemixture sterilizers; 2 in. x 3/4 in. (5,1 cm x 1,9 cm)

1244B EO Chemical Integrator; moving front; for gas 100 each/bag 10 bags/casemixture sterilizers; 2 in. x 3/4 in. (5,1 cm x 1,9 cm)

1244E EO Chemical Integrator; moving front with extender; 1000 each/bag 1 bag/casefor gas mixture sterilizers; 9 in. x 3/8 in. (22,9 cm x 1,0 cm)

1240E Extender only; 2500 each/bag 2 bags/case7-1/2 in. x 3/8 in. (19,1 cm x 1,0 cm)

Low Temperature Chemical Indicators

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Chemical Indicator Roll

Chemical indicators for steam in a roll. The chemical indicator lines will turndark brown when exposed to steam.

3M™ Comply™ Indicator Roll*


1201** Steam (60 yards) 10 rolls/box 1 box/case

*Contains Dry Natural Rubber**Can be used with 3M tape dispenser 1206 (see page 27 )

For use in all steam sterilizers. Long stripe of chemicalindicator ink printed on perforated-style strip. Allowsfull- or half-length use for different pack sizes. Utilizesdistinct color change to indicate process results.Indicator changes color from white to dark brown/black(dark or darker than the color block located in center ofstrip) when exposed to steam sterilization conditions.

3M™ Comply™ Steam Chemical Indicator Strip


1250 Steam Chemical Indicator Strip 240 each/box 8 boxes/case5/8 in. x 8 in. (1,5 cm x 20 cm)

For use in all steam sterilizers. Chemical indicatorprinted as block on one end of short or long strip.Indicator changes color to dark brown/black (blockturns as dark or darker than a color standard) whenexposed to steam sterilization conditions.

3M™ Comply™ Steam Chemical Indicator Strips


00107 Long Form, 250 each/box 20 boxes/case5/8 in. x 8-1/2 in. (1,5 cm x 22 cm)

00107A Long Form—Economy Pack 1000 each/box 4 boxes/case5/8 in. x 8-1/2 in. (1,5 cm x 22 cm)

00109 Short Form, 250 each/box 20 boxes/case5/8 in. x 4-1/4 in. (1,5 cm x 11 cm)

00109A Short Form—Economy Pack 1000 each/box 4 boxes/case5/8 in. x 4-1/4 in. 1,5 cm x 11 cm)



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Dry Heat Chemical Indicators

Sterilization monitor for dry heat sterilizers. Indicator changes color from tan toblack within 5 minutes at 170˚C (340˚F) during exposure to dry heat processing.

3M™ Comply™ Dry Heat Chemical Indicator Strip


00311 Dry Heat Chemical Indicator Strip 250 each/box 10 boxes/case5/8 in. x 4-1/4 in. (1,5 cm x 11 cm)

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Low Temperature Chemical Indicators (continued)

For use in 100% EO and EO/HCFC gas mixtures. Long stripe of chemical indicator ink printed onperforated-style strip. Allows full- or half-length use for different pack sizes. Indicator changes color fromburgundy red to green when exposed to ethylene oxidesterilization conditions.

3M™ Comply™ EO Chemical Indicator Strip


1251 EO Chemical Indicator Strip; 240 each/box 4 boxes/case5/8 in. x 8 in. (1,5 cm x 20 cm)

For use in 100% EO and EO/HCFC gas mixtures. Chemical indicatorink printed as a block on one end of short or long strips. Available inplastic-laminated and non-laminated, economy pack styles. Indicatorchanges color from yellow to blue when exposed to ethylene oxidesterilization conditions.

3M™ Comply™ EO Chemical Indicator Strips


00152 Short Form—Economy Pack 800 each/box 4 boxes/caseNon-laminated strips5/8 in. x 4-1/4 in. (1,5 cm x 11 cm)

00155 Short Form—Economy Pack 200 each/box 20 boxes/casePlastic-laminated strips5/8 in. x 4-1/4 in. (1,5 cm x 11 cm)

Chemical Indicator Roll

Chemical indicators for EO gas in a roll. The chemical indicator lines will turnred when exposed to EO gas.

3M™ Comply™ Indicator Roll*


1202** Ethylene Oxide (60 yards) 10 rolls/box 1 box/case

*Contains Dry Natural Rubber**Can be used with 3M tape dispenser 1206 (see page 27 )

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Protects sharp-pointed surgical instruments from damage and reduces possibilityof pouch puncture during sterilization and handling. Indicators on the protectorsverify steam or EO gas processing.

3M™ Comply™ Instrument Protectors


13911 2 in. x 5 in. (5,1 cm x 12,8 cm) 100/pack 10 packs/case

13913 3-1/2 in. x 6-5/8 in. (9,9 cm x 16,8 cm) 100/pack 10 packs/case

13915 5-1/2 in. x 9-1/2 in. (14 cm x 24 cm) 100/pack 10 packs/case

Instrument Protectors

Sterilization Indicator Labels

Peel-off, pressure-sensitive labels for hard-surfaced items such as unwrappedglass or metal.

3M™ Comply™ Chemical Indicator Labels


00162 Steam/EO Gas— 1000 labels/roll 12 rolls/caseCombination label for steam or EO gas sterilizers. Steam 1 roll/boxindicator bar changes color from blue to black during steam sterilization. EO gas indicator changes color fromyellow to rust/red during EO gas sterilization.

00160 Steam—For steam sterilizers. Color changes from purple 1000 labels/roll 12 rolls/caseto green during steam sterilization. 1 roll/box

00170 Dry Heat—For use in dry heat sterilizers 170˚C 1000 labels/roll 12 rolls/case(340˚F) or above. The indicator ink on the label 1 roll/boxturns from tan to black within 5 minutes at 170˚C(340˚F) to verify exposure during dry heat sterilization.

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Each monitor consists of a plastic strip with a black-framed chemical reactionpad. Pad changes from white to yellow when dipped in glutaraldehyde solutionswith adequate concentration.

3M™ Comply™ Glutaraldehyde Monitors, 1.5%, 1.8%, 2.1%

Designed to test glutaraldehyde solutions with stated manufacturer’s MinimumEffectiveness Concentration (MEC) values. Indicates safe solutions when above1.5%, 1.8% or 2.1% MECs.


3983MM 1.5% MEC* 60 monitors/bottle 2 bottles/case

3987 1.8% MEC* 60 monitors/bottle 2 bottles/case

3989 2.1% MEC* 60 monitors/bottle 2 bottles/case

*Test strips are brand specific. Please contact 3M for details.

Each monitor contains a black-framed pad which turns yellow when a glutaraldehyde solution is above 1% concentration.

3M™ Comply™ Glutaraldehyde Monitors, 2% to 3.5%

Designed for glutaraldehyde solutions with starting concentrations of 2% to3.5%, but not labeled for specific MECs. Indicates safe solutions when above1% effective concentrations.


3552 - 60 monitors/bottle 12 bottles/case

3553 - 60 monitors/bottle 2 bottles/case

Glutaraldehyde Monitors

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Equ ipmen t Con t ro l

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Bowie-Dick Plus Test Pack features the Early Warning Test Sheet that identifies potential air leaks or vacuum pump failures before they appear on the Bowie-Dick test sheet.

3M™ Comply™ Bowie-Dick Plus Test Pack with Early Warning Test Sheet


00135 Comply Bowie-Dick Plus Test Pack with 20 packs/box 4 boxes/caseEarly Warning Test Sheet

Bowie-Dick Plus Test Pack with Early Warning Test Sheet

Designed for vacuum-assisted sterilizers to test the efficacy of the vacuumsystem, to remove air from the sterilizer chamber and to detect leaks in the system that would allow air into the chamber.

• Bowie-Dick test packs make testing steam penetration and air removal,as well as detecting air leaks, more convenient and cost effective

• Designed to give equivalent results to those obtainable by the Bowie and Dick protocol

• Preassembled packs reduce both labor and material costs

• Indicator pattern is easy to read and interpret

3M™ Comply™ Bowie-Dick Type Test Pack


1233 Comply Disposable Test Pack 6 packs/bag 5 bags/case

3M™ Comply™ Bowie-Dick Test Sheets


00130 Comply Internal Steam Indicator Sheets 50 sheets/box 5 boxes/case

Bowie-Dick Type Test Packs and Sheets

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Bowie-Dick Test Packs


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Indicator Tape for Steam Sterilization

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A reliable steam indicator tape that provides immediate identification ofprocessed items and also serves as a closure tape to seal sterilization packs. The chemical indicator lines will turn dark when exposed to a steam sterilization process.

• Reliable chemical indicator responds when exposed to a steam sterilization process

• Adheres to woven, treated woven, non-woven, paper and paper/plastic wraps

• Adhesive seals packs securely, but is easy to remove

• Backing stretches to minimize tape pop-off during pack sterilization

• Can be written on or labeled with preprinted labels such as 3M™ Comply™

Sterilization Record Labels (page 31)

3M™ Comply™ Indicator Tape for Steam Sterilization*


1222-0N 1/2 in. x 60 yd. (1,25 cm x 55 m) - 36 rolls/caseWhite

1222-1N 1 in. x 60 yd. (2,5 cm x 55 m) - 18 rolls/caseWhite

1222-2N 2 in. x 60 yd. (5 cm x 55 m) - 10 rolls/caseWhite

1222-6N 3/4 in. x 60 yd. (1,9 cm x 55 m) - 24 rolls/caseWhite

*Contains Dry Natural Rubber.


Indicator Tapes

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Indicator Tape Dispensers

1206 Tape Dispenser

The 1206 tape dispenser has a weighted base and is capable of handling two 1-inch rolls or one 2-inch roll of indicator tape, or one 2-inch Comply indicator roll.


1206 Weighted base, holds 2 rolls - 1 each/case

C22 Heavy Duty Tape Dispenser

The C22 heavy duty tape dispenser is made of rugged, high-impact, durable plastic and iscapable of handling two rolls of 1-inch wide indicator tape.


C22 Heavy duty, holds 2 rolls - 2 each/case

M51/M51-T Tape Dispenser

The M51 tape dispenser holds one indicator tape roll up to 1 inch in width. The M51-T isthe same as the M51 dispenser with the addition of the tabber attachment, whichautomatically folds a 1/4-inch length of tape for easy handling and removal.


M51 Without tabber - 6 each/case

M51-T With tabber - 6 each/case

M96 Definite-Length Tape Dispenser

The M96 definite-length tape dispenser adjusts to allow consistent dispensing of indicatortape strips, up to 5 inches in length. Holds one indicator tape roll up to 1 inch in width.


M96 Definite length (with wheel accessory) - 6 each/case

M920 Definite-Length Tape Dispenser

The M920 definite-length tape dispenser adjusts to allow consistent dispensing of indicatortape strips, up to 4 inches in length. Holds one indicator tape roll up to 1 inch in width.


M920 Definite length - 6 each/case


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A reliable steam indicator tape specifically designed for disposable wraps thatprovides immediate identification of processed items and also serves as a closureto seal sterilization packs. The chemical indicator lines will turn dark whenexposed to a steam sterilization process.

• “Blue tape” is the industry’s first indicator tape for disposable wraps

• Aggressive adhesive secures packs wrapped with disposable materials

• Uses the same reliable chemical indicator as 3M™ Comply™ 1222Indicator Tape




3M™ Comply™ Steam Indicator Tape for Disposable Wraps*


1255-1N 1 in. x 60 yd. (2,5 cm x 55 m) - 18 rolls/caseTape for Steam

1255-6N 3/4 in. x 60 yd. (1,9 cm x 55 m) - 24 rolls/caseTape for Steam


Steam Indicator Tape for Disposable Wraps



A reliable ethylene oxide gas indicator tape that instantly identifies items that have been exposed to EO gas and also serves as a closure tape to sealsterilization packs. The chemical indicator lines will turn red when exposed to an EO sterilization process.

• Adhesive seals packs securely, but is easily removed, leaving no adhesive residue

• Color change verifies exposure to ethylene oxide gas




3M™ Comply™ Indicator Tape for Ethylene Oxide Sterilization*


1224-0 1/2 in. x 60 yd. - 36 rolls/case(1,25 cm x 55 m)

1224-1 1 in. x 60 yd. - 18 rolls/case(2,5 cm x 55 m)

1224-6 3/4 in. x 60 yd. - 24 rolls/case(1,9 cm x 55 m)


Indicator Tape for Ethylene Oxide (EO) Sterilization

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Record Keep ing

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An efficient and secure system for all sterilization process monitoringdocumentation. Easily and accurately record, review, archive, and retrievesterilization process monitoring data. Use to consolidate all sterilization process data into an easily accessible database. Regular compliance promptshelp maintain compliance with JCAHO and other recommended standards.

3M™ Record Keeping Software


1213A Record Keeping Software - 1 each/case

Please contact your 3M Sales Representative for ordering information about this product.

Record Keeping Software

Log Books, Envelopes and Record Charts



Complete record keeping systems that maintain your sterilization processinformation and reduce record keeping time to just minutes each day. The preprinted log books put all the information you need to help you meet requirements at your fingertips.

3M™ Log Book and Envelopes


1254B Sterilization Log Book for envelopes (empty) - 1 each/case

1254E-F 100 flash envelopes for 1254B Log Book 100 each/pack 5 packs/case

1254E-S 100 steam envelopes for 1254B Log Book 100 each/pack 5 packs/case

1254E-LT 100 low temperature envelopes for 1254B Log Book 100 each/pack 5 packs/case

3M™ Log Books and Record Sheets


1266 Steam Log Book (small sheets) - 1 each/case

1266S 50 replacement sheets for 1266 Log Book 50 each/pack 1 pack/case

1268 Low Temperature Log Book (small sheets) - 1 each/case


1283 Glutaraldehyde Log Book (small sheets) - 1 each/case


Record Keeping

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Record Keep ing

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3M™ Comply™ Label Gun


1256B Printing applicator—prints and applies labels 1 each/box 1 box/casedirectly where needed

Event Related Sterilization Record Labels—“Sterilized”


1269B Blue labels; 1125 labels/roll 1 box/case1-1/8 in. x 5/8 in. (2,85 cm x 1,58 cm) 12 rolls/box

1269BL Black labels; 1125 labels/roll 1 box/case1-1/8 in. x 5/8 in. (2,85 cm x 1,58 cm) 12 rolls/box

1269G Green labels; 1125 labels/roll 1 box/case1-1/8 in. x 5/8 in. (2,85 cm x 1,58 cm) 12 rolls/box

1269R Red labels; 1125 labels/roll 1 box/case1-1/8 in. x 5/8 in. (2,85 cm x 1,58 cm) 12 rolls/box

Sterilization Record Labels—“Expires”


1257B Blue labels; 1125 labels/roll 1 box/case1-1/8 in. x 5/8 in. (2,85 cm x 1,58 cm) 12 rolls/box

1257BL Black labels; 1125 labels/roll 1 box/case1-1/8 in. x 5/8 in. (2,85 cm x 1,58 cm) 12 rolls/box

1257BR Brown labels;. 1125 labels/roll 1 box/case1-1/8 in. x 5/8 in (2,85 cm x 1,58 cm) 12 rolls/box

1257G Green labels; 1125 labels/roll 1 box/case1-1/8 in. x 5/8 in. (2,85 cm x 1,58 cm) 12 rolls/box

1257GD Gold labels; 1125 labels/roll 1 box/case1-1/8 in. x 5/8 in. (2,85 cm x 1,58 cm) 12 rolls/box

1257GY Grey labels; 1125 labels/roll 1 box/case1-1/8 in. x 5/8 in. (2,85 cm x 1,58 cm) 12 rolls/box

1257OR Orange labels; 1125 labels/roll 1 box/case1-1/8 in. x 5/8 in. (2,85 cm x 1,58 cm) 12 rolls/box

1257P Purple labels; 1125 labels/roll 1 box/case1-1/8 in. x 5/8 in. (2,85 cm x 1,58 cm) 12 rolls/box

1257PK Pink labels; 1125 labels/roll 1 box/case1-1/8 in. x 5/8 in. (2,85 cm x 1,58 cm) 12 rolls/box

1257R Red labels; 1125 labels/roll 1 box/case1-1/8 in. x 5/8 in. (2,85 cm x 1,58 cm) 12 rolls/box

1257Y Yellow labels; 1125 labels/roll 1 box/case1-1/8 in. x 5/8 in. (2,85 cm x 1,58 cm) 12 rolls/box

Labels Contain Dry Natural Rubber

Sterilization Record Labels—Blank


1257W White labels; 1125 labels/roll 1 box/case1-1/8 in. x 5/8 in. (2,85 cm x 1,58 cm) 12 rolls/box

Labels Contain Dry Natural Rubber

Label Gun System


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Load Record Cards

For steam and EO gas sterilizers. Provides a permanent record of sterilizer useand work flow.

3M™ Comply™ Load Record Cards


1252 Steam load record card 240 each/box 4 boxes/case3 in. x 5 in. (7,6 cm x 12,8 cm)

1253 EO load record card 240 each/box 2 boxes/case3 in. x 5 in. (7,6 cm x 12,8 cm)

67200 Steam and EO load record card 250 each/box 4 boxes/case3 in. x 5 in. (7,6 cm x 12,8 cm)

67201 Steam and EO load record card 250 each/box 4 boxes/case4 in. x 5-1/2 in. (10,2 cm x 14 cm)



Sterilization Integrator Load Record Card

A single-use device that indicates whether materials within a pack or load havebeen exposed to conditions necessary for sterilization. The steam sterilizationrecord cards can be used in vacuum, gravity and flash sterilizers.

3M™ Comply™ Load Record Card


4171MM Integrator with Load Record Card—Steam 100 each/box 1 box/case


Ste r i l i za t i on Assu rance

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An effective multi-enzyme detergent used for cleaning metallic and plasticmedical instruments, including flexible and rigid endoscopes, and dentalinstruments. Effectively digests human secretions after immersion for only 2–10 minutes. Made with biodegradable materials.

3M™ Rapid Multi-Enzyme Detergent


70500-B 5 liter bottle 3 each/case case

70500-D 1 liter bottle 12 each/case case

70500-H 100ml bottle 40 each/case case

Multi-Enzyme Detergent


Cleaning and Decontamination

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These dual-cycle, 100% EO gas sterilizer/aerators have 4.0 cu. ft. (4XL) and 4.8 cu. ft. (5XL) chambers.

• 100% Ethylene Oxide—proven effective and trusted by health care providersworldwide for sterilization of heat and/or moisture-sensitive devices

• Video screen technology shows cycle status

• Single unit-dose EO cartridge is punctured inside the negative-pressurechamber only when proper chamber conditions are achieved

• Continuous temperature monitoring maintains temperature of the selectedcycle and automatically shuts off if the temperature exceeds setpoint

• Programmable access codes allow you to monitor and trace cycle operator

• Built-in aeration cycle

• Relative humidity detection and documentation (optional)

3M™ Steri-Vac™ 4XL and 5XL Sterilizer/Aerators

Cat. # Description Shipping

4XL Sterilizer/aerator 1 unit/caseChamber: 16-1/8" (H) x 18-1/8" (W) x 24" (D)

41 cm (H) x 46 cm (W) x 61 cm (D)

5XL Sterilizer/aerator 1 unit/caseChamber: 15" (H) x 17" (W) x 33-3/4"(D)

38 cm (H) x 43 cm (W) x 83 cm (D)

The model 8XL dual-cycle 100% EO gas sterilizer/ aerator has a 7.9 cu. ft.chamber. In addition to all of the benefits of the 4XL and 5XL, the 8XL provides:

• 100% Ethylene Oxide—proven effective and trusted by health care providersworldwide for sterilization of heat and/or moisture-sensitive devices

• Dependable computer controlled electronic design provides accuracy—automatically stops cycle and displays error code if error is detected

• Relative humidity feature continuously monitors, maintains and documentsthe proper humidity in the sterilization chamber during the precondition phase

3M™ Steri-Vac™ 8XL Sterilizer/Aerator


8XL Sterilizer/aerator 1 unit/caseExterior: 70" (H) x 37" (W) x 43" (D)

179 cm (H) x 94 cm (W) x 109 cm (D)Chamber: 18-1/8" (H) x 20" (W) x 38" (D)

46 cm (H) x 51 cm (W) x 97 cm (D)

Gas Sterilizers/Aerators

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Sterilization Hardware




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Transfer Cart

A stainless steel transfer cart developed to assist operators to move, lift or lower materials and supplies around the Central Service/Sterile Processing Department.

• Table top extends up to 142,2 cm (56 in.) to accommodate load transfer

• Stainless steel table top provides durable surface

• Upper table pedal slowly raises the height of cart’s table top

• Lower table pedal allows for controllable lowering of table top

• Brake actuation pedal secures cart placement

3M™ Transfer Cart


6010 Transfer Cart 1 cart/caseTable size: 18-1/2" x 35" (47 cm x 89 cm); 19-3/4" x 35" (50 cm x 89 cm) for 8XL Kit Holding capacity: 68 kg

Aerator

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The model XL aeration cabinet circulates warm, filtered air in its 5 cu. ft.chamber. Designed for compatibility with Steri-Vac sterilizers.

• Two selectable aeration temperatures, 37˚C (99˚F) or 55˚C (131˚F)

• Modular system for versatility

• Space efficient

• A door lock prevents unauthorized access

3M™ Steri-Vac™ XL Aerator


XL Aerator 1 unit/caseExterior: 24-3/8" (H) x 30-3/4" (W) x 36-5/8" (D)

62 cm (H) x 78 cm (W) x 93 cm (D)Chamber: 16-1/8" (H) x 18-1/8" (W) x 33" (D)

41 cm (H) x 46 cm (W) x 84 cm (D)




Drying Cabinet

The model 45 dramatically reduces the time required to dry inhalation therapyand anesthesia equipment to between one-half and three hours.

• Capacity for drying 45 tubes from 6 mm (1/4 in.) to 44 mm (1-3/4 in.) indiameter at one time

• Removable wire basket for drying small parts in one-half of the cabinet, whiledrying tubing in the other half

• Capacity for holding four baskets— two deep on each side of the cabinet ortwo double baskets across the cabinet

• Dries tubes in a fraction of the time

3M™ Steri-Vac™ Drying Cabinet


45AA Drying Cabinet with wall mounting bracket 1 unit/case68-7/8" (H) x 22-3/8" (W) x 15-1/2" (D)175 cm (H) x 57 cm (W) x 42 cm (D)

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The abator removes EO gas exhausted from 3M™ Steri-Vac™ sterilizers and aerators, converting it into CO2 and water vapor. At normal operatingtemperatures and concentrations, removal efficiency is 99.9+%.

• Works automatically with sterilization system

• Interfaces with up to two sterilizers

3M™ EtO-Abator System


50SCFM Abator 1 unit/case31" (H) x 32" (W) x 41" (D)80 cm (H) x 82 cm (W) x 105 cm (D)

3M™ EtO-Abator System

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3M™ Steri-Lok™ Closure Tape


1225 White flatback paper tape 18 rolls/case case1 in. x 60 yd. (2,5 cm x 55 m)

3M™ Steri-Lok™ Peel Open Packages for EO Gas Sterilization (Film/Tyvek)


8501 3-1/8 in. x 7-7/8 in. (7,9 cm x 20 cm) 250 each/box 4 boxes/case

8502 3-7/8 in. x 9-3/4 in. (7,9 cm x 24,8 cm) 250 each/box 4 boxes/case

8503 5-7/8 in. x 9-3/4 in. (14,9 cm x 24,8 cm) 250 each/box 4 boxes/case

8504 3-1/8 in. x 24 in. (7,9 cm x 61 cm) 250 each/box 4 boxes/case

8505 7 in. x 13 in. (17,8 x 33 cm) 250 each/box 2 boxes/case

8506 11-3/4 in. x 14-7/8 in. (29,8 cm x 38 cm) 250 each/box 2 boxes/case

8507 15-3/4 in. x 18 in. (40 cm x 45,7 cm) 250 each/box 2 boxes/case

3M™ Steri-Lok™ Polyethylene Bags for EO Gas Sterilization


8250 3-1/4 in. x 5-1/2 in. (8,3 cm x 14 cm) 100 each/pack 5 packs/case

8251 7 in. x 13 in. (17,8 cm x 33 cm) 100 each/pack 5 packs/case

8252 9 in. x 17 in. (22,9 cm x 43,2 cm) 100 each/pack 5 packs/case


8254 15 in. x 23 in. (38 cm x 58,4 cm) 100 each/pack 5 packs/case


3M™ Steri-Lok™ Polyethylene Tubes for EO Gas Sterilization


8203 3 in. x 75 ft. (7,6 cm x 22,9 m) 1 each/box 4 boxes/case




Packaging

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EO Monitoring Badge

Lightweight badge packed with ethylene oxide-sensitive material. Clips to lapel or pocket near breathing zone for passive monitoring of individual during a work shift. Monitor is mailed for analysis. Report is mailed to user (or telephoned if permissible exposure limits are exceeded).

3M™ EO Monitoring Badge


3550 EO Monitoring Badge - 5 each/case




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Printer Paper

3M™ Steri-Vac™ Printer Paper


1215A Printer Paper, 51 mm (2 inch) wide, 2 rolls/casefor models 400B & 400C

1216A Printer Paper, 60 mm (2-3/8 inch) wide, 2 rolls/casefor 4XL and 5XL (w ser# below 720000)

1217 Printer Paper, 79 mm (3-1/8 inch) wide, 2 rolls/casefor 8XL and 5XL (w ser# above 720000)

EO Gas Cartridges

100% ethylene oxide (EO) is contained in a single-dose cartridge. The cartridge contains 3.5, 4.5 or 6 oz. of EO depending on the model Steri-Vac sterilizer used.

• The system provides an easy, cost-effective and efficient method of gas sterilization

• Only small amounts of ethylene oxide are contained in the cartridges

• Precise usage of EO with single-dose cartridges means no waste of sterilant

• With Steri-Gas cartridges, operators have no bulky, heavy gas tanks to handle,and no hoses, valves and filters to adjust or replace

• The cartridges do not contain CFCs or HCFCs

3M™ Steri-Gas™ Cartridges


4-100 100 gram cartridge for models 400C, 4XL and 5XL 12 each/box 4 boxes/case

4-134 127 gram cartridge for model 400B 12 each/box 4 boxes/case

8-170 170 gram cartridge for model 8XL 12 each/box 4 boxes/case

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00107 3M™ Comply™ Steam Chemical Indicator Strip 16

00107A 3M™ Comply™ Steam Chemical Indicator Strip 16


00109A 3M™ Comply™ Steam Chemical Indicator Strip 16

00117 3M™ Comply™ Steam Chemical Indicator-Plus Strip 15

00118 3M™ Comply™ Steam Chemical Indicator Plus Strip 15

00119 3M™ Comply™ Steam Chemical Indicator Plus Strip 15

00130 3M™ Comply™ Bowie-Dick Test Sheets 23

00135 3M™ Comply™ Bowie-Dick Plus Test Pack with Early Warning Test Sheet 23

00152 3M™ Comply™ EO Chemical Indicator Strip 18


00160 3M™ Comply™ Chemical Indicator Label 21



4-100 3M™ Steri-Gas™ Cartridge 38



4XL 3M™ Steri-Vac™ 4XL Sterilizer/Aerator 35



45AA 3M™ Steri-Vac™ Drying Cabinet 37

50SCFM 3M™ EtO-Abator System 36

115 3M™ Attest™ Biological Indicator Monitoring Starter Kit 10

116 3M™ Attest™ Biological Indicator Incubator 10





190 3M™ Attest™ 190 Auto-reader 8

290 3M™ Attest™ 290 Auto-reader 8

1201 3M™ Comply™ Indicator Roll (Steam) 16

1202 3M™ Comply™ Indicator Roll (EO) 18

1206 1206 Tape Dispenser 27

1215A 3M™ Steri-Vac™ Printer Paper 38

1216A 3M™ Steri-Vac™ Printer Paper 38

1217 3M™ Steri-Vac™ Printer Paper 38

1222-0N 3M™ Comply™ Indicator Tape for Steam Sterilization 25




1224-0 3M™ Comply™ Indicator Tape for Ethylene Oxide Sterilization 26



1233 3M™ Comply™ Bowie-Dick Type Test Pack 23

1240E 3M™ Comply™ (SteriGage™) Integrator Extender 15 &17

Index by Catalog Number

Catalog Number Product Name Page Number

Index


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1269G Event Related Sterilization Record Labels—“Sterilized” 31

1269R Event Related Sterilization Record Labels—“Sterilized” 31

1276 3M™ Attest™ Biological Indicator Test Pack for 250°F/121°C Gravity and 270°F/132°C Vacuum-Assisted Steam Sterilizer 9

1276F 3M™ Attest™ Biological Indicator Test Pack for 250°F/121°C Gravity and 270°F/132°C Vacuum-Assisted Steam Sterilizer 9

1278 3M™ Attest™ Biological Indicator Test Pack for Ethylene Oxide 9

1278F 3M™ Attest™ Biological Indicator Test Pack for Ethylene Oxide 9

1283 3M™ Glutaraldehyde Log Book 29

1283S Replacement Sheets for 1283 Log Book 29

1291 3M™ Attest™ Rapid Readout Biological Indicator for 270°F/132°C Gravity Displacement Steam Sterilizer 7

1292 3M™ Attest™ Rapid Readout Biological Indicator for 250°F/121°C Gravity and 270°F/132°C Vacuum-Assisted Steam Sterilizer 7

1296 3M™ Attest™ Rapid Readout Biological Indicator Test Pack for 250°F/121°C Gravity and 270°F/132°C Vacuum-Assisted Steam Sterilizer 7

1296F 3M™ Attest™ Rapid Readout Biological Indicator Test Pack for 250°F/121°C Gravity and 270°F/132°C Vacuum-Assisted Steam Sterilizer 7

13911 3M™ Comply™ Instrument Protector 21



2482 3M™ Enzymatic Indicators 12

2482T 3M™ Enzymatic Indicators 12

2482F 3M™ Enzymatic Indicators 12

2483 3M™ Challenge Packs 12

2486 3M™ Enzymatic Indicators and Challenge Packs 12

2486F 3M™ Enzymatic Indicators and Challenge Packs 12

3550 3M™ EO Monitoring Badge 39

3552 3M™ Comply™ Glutaraldehyde Monitor 20

3553 3M™ Comply™ Glutaraldehyde Monitor 20

3983MM 3M™ Comply™ Glutaraldehyde Monitor, 1.5% 20

3987 3M™ Comply™ Glutaraldehyde Monitor, 1.8% 20

3989 3M™ Comply™ Glutaraldehyde Monitor, 2.1% 20

41360 3M™ Comply™ (SteriGage™) Steam Chemical Integrator Test Pack 14

41380 3M™ Attest™ Steam-Plus Test Pack 9

4171MM 3M™ Comply™ Load Record Cards 30

45260 3M™ Comply™ (SteriGage™) EO Chemical Integrator Test Pack 14

6010 3M™ Transfer Cart 37

67200 3M™ Comply™ Load Record Cards (Steam and EO) 30

67201 3M™ Comply™ Load Record Cards (Steam and EO) 30

70500-B 3M™ Rapid Multi-Enzyme Detergent, 5 liter bottle 33

70500-D 3M™ Rapid Multi-Enzyme Detergent, 1 liter bottle 33

70500-H 3M™ Rapid Multi-Enzyme Detergent, 100 ml bottle 33

78-2007-2981-5 3M™ Attest™ 290 Auto-reader Power Cord 8

78-8078-7349-8 3M™ Attest™ 190 Auto-reader UV Bulb and Starter Kit 8

8203 3M™ Steri-Lok™ Polyethylene Tube for EO Gas Sterilization, 3 in. x 75 ft. (7,6 cm x 2287,5 cm) 39



1243A 3M™ Comply™ (SteriGage™) Steam Chemical Integrator 15

1243B 3M™ Comply™ (SteriGage™) Steam Chemical Integrator 15

1243E 3M™ Comply™ (SteriGage™) Steam Chemical Integrator 15

1244A 3M™ Comply™ (SteriGage™) EO Chemical Integrator 17

1244B 3M™ Comply™ (SteriGage™) EO Chemical Integrator 17

1244E 3M™ Comply™ (SteriGage™) EO Chemical Integrator 17

1248 3M™ Comply™ Gas Plasma Chemical Indicator Strip 17

1249 3M™ Comply™ Liquid Peracetic Acid Chemical Indicator 17



1252 3M™ Comply™ Load Record Card (Steam) 30

1253 3M™ Comply™ Load Record Card (EO) 30

1254B 3M™ Sterilization Log Book for Envelopes 29

1254E-F Flash Envelopes for 1254B Log Book 29

1254E-LT Low Temperature Envelopes for 1254B Log Book 29

1254E-S Steam Envelopes for 1254B Log Book 29

1255-1N 3M™ Comply™ Steam Indicator Tape for Disposable Wrap 26

1255-6N 3M™ Comply™ Steam Indicator Tape for Disposable Wrap 26

1256B 3M™ Comply™ Label Gun 31

1257B Sterilization Record Labels—“Expires” 31

1257BL Sterilization Record Labels—“Expires” 31

1257BR Sterilization Record Labels—“Expires” 31

1257G Sterilization Record Labels—“Expires” 31

1257GD Sterilization Record Labels—“Expires” 31

1257GY Sterilization Record Labels—“Expires” 31

1257OR Sterilization Record Labels—“Expires” 31

1257P Sterilization Record Labels—“Expires” 31

1257PK Sterilization Record Labels—“Expires” 31

1257R Sterilization Record Labels—“Expires” 31

1257W Sterilization Record Labels—Blank 31

1257Y Sterilization Record Labels—“Expires” 31

1261 3M™ Attest™ Biological Indicator for 270°F/132°C Gravity Displacement Steam Sterilizer 9

1261P 3M™ Attest™ Biological Indicator for 270°F/132°C Gravity Displacement Steam Sterilizer 9

1262 3M™ Attest™ Biological Indicator for 250°F/121°C Gravity and 270°F/132°C Vacuum-Assisted Steam Sterilizer 9

1262P 3M™ Attest™ Biological Indicator for 250°F/121°C Gravity and 270°F/132°C Vacuum-Assisted Steam Sterilizer 9

1264 3M™ Attest™ Biological Indicator for Ethylene Oxide 9

1264P 3M™ Attest™ Biological Indicator for Ethylene Oxide 9

1266 3M™ Steam Log Book 29

1266S Replacement Sheet for 1266 Log Book 29

1268 3M™ Low Temperature Log Book 29

1268S Replacement Sheet for 1268 Log Book 29

1269B Event Related Sterilization Record Labels—“Sterilized” 31

1269BL Event Related Sterilization Record Labels—“Sterilized” 31




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8250 3M™ Steri-Lok™ Polyethylene Bags for EO Gas Sterilization, 3-1/4 in. x 5-1/2 in. (8,3 cm x 14 cm) 39

8251 3M™ Steri-Lok™ Polyethylene Bags for EO Gas Sterilization, 7 in. x 13 in. (17,8 cm x 33 cm) 39

8252 3M™ Steri-Lok™ Polyethylene Bag for EO Gas Sterilization, 9 in. x 17 in. (22,9 cm x 43,2 cm) 39

8253 3M™ Steri-Lok™ Polyethylene Bag for EO Gas Sterilization, 12 in. x 15 in. (30,5 cm x 38 cm) 39

8254 3M™ Steri-Lok™ Polyethylene Bag for EO Gas Sterilization, 15 in. x 23 in. (38 cm x 58,4 cm) 39

8255 3M™ Steri-Lok™ Polyethylene Bag for EO Gas Sterilization, 20 in. x 30 in. (50,9 cm x 76 cm) 39

8501 3M™ Steri-Lok™ Peel Open Package for EO Gas Sterilization, 3-1/8 in. x 7-7/8 in. (7,9 cm x 20 cm) 39

8502 3M™ Steri-Lok™ Peel Open Package for EO Gas Sterilization, 3-7/8 in. x 9-3/4 in. (7,9 cm x 24,8 cm) 39

8503 3M™ Steri-Lok™ Peel Open Package for EO Gas Sterilization, 5-7/8 in. x 9-3/4 in. (14,9 cm x 24,8 cm) 39

8504 3M™ Steri-Lok™ Peel Open Package for EO Gas Sterilization, 3-1/8 in. x 24 in. (7,9 cm x 61 cm) 39

8505 3M™ Steri-Lok™ Peel Open Package for EO Gas Sterilization, 7 in. x 13 in. (17,8 cm x 33 cm) 39

8506 3M™ Steri-Lok™ Peel Open Package for EO Gas Sterilization, 11-3/4 in. x 14-7/8 in. (29,8 cm x 38 cm) 39

8507 3M™ Steri-Lok™ Peel Open Package for EO Gas Sterilization, 15-3/4 in. x 18 in. (40 cm x 45,7 cm) 39

C22 C-22 Heavy Duty Tape Dispenser 27

M51 M51/M51-T Tape Dispenser without tabber 27

M51-T M51/M51-T Tape Dispenser with tabber 27

M920 M920 Definite-Length Tape Dispenser 27

M96 M96 Definite-Length Tape Dispenser 27

XL 3M™ Steri-Vac™ XL Aerator 36




3M Infection

Prevention

TM

SterilizationAssurance

SkinPrep

Sterile Field & Surface

EnvironmentalCleaning

WoundManagement

A full line of innovative products that enhance patientoutcomes and help manage health care costs.

3Health Care

3M Center, Building 275-4W-02St. Paul, MN 55144-1000 USA1 800 [email protected]/healthcare

3M Canada

Post Office Box 5757London, Ontario N6A 4T1Canada1 800 563-2921

Minimum 10% Post-Consumer Fiber

Steris System 1 is a registeredtrademark of Steris Corporation.STERRAD is a registered trademarkof Johnson & Johnson, Inc.

H.I. 4509Printed in U.S.A.© 3M 2002 All Rights Reserved70-2009-0360-0


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