Simpli Germicidal Disposable Wipes 6″ x 6.75″ 160 ct (Case of 12 )

EFFICACY

BACTERIAL ORGANISM EFFICACY

MULTI-DRUG RESISTANT BACTERIA

• Acinetobacter baumannii [ATCC 19606]
• Enterobacter cloacae NDM-1 positive [CDC 1000654]
• ESBL Producing Escherichia coli (E. coli) [ATCC BAA-196]
• Klebsiella pneumoniae KP02 positive, ST258 (multi-drug and carbapenem resistant)
• [CDC 2008030]
• Methicillin Resistant Staphylococcus aureus (M RSA) [ATCC 33592]
• Vancomycin Resistant Enterococcus faecalis (VRE) [ATCC 51299]

Test Method Used: Modified AOAC Germicidal Spray Method for Hard Surface Disinfection
Organic Soil Load: 5% Horse Serum or 5% Fetal Bovine Serum
Exposure Time: 2 minutes at 68-77°F
Incubation: 48 hours +/- 2 hours at 95-98.6°F
Results: No growth observed

BACTERIA

• Bordetella pertussis [ATCC 12743]
• Burkholderia cepacia [ATCC 25416]
• Campylobacterje/uni [ATCC 29428]
• Escherichia coli (E. coli) [ATCC 11229]
• Escherichia coli 0 1 57: H7 [ATCC 35150]
• Klebsiella pneumoniae [ATCC 4352]
• Pseudomonas aeruginosa [ATCC 15442]
• Salmonella enterica [ATCC 10708]
• Staphylococcus aureus [ATCC 6538]

Test Method Used: Modified AOAC Germicidal Spray Method for Hard Surface Disinfection
Organic Soil Load: 5% Horse Serum or 5% Fetal Bovine Serum
Exposure Time: 2 minutes at 66-77°F
Incubation: 48 hours +/- 2 hours to 6 days at 86-98.6°F
Results: No growth observed

MYCOBACTERIUM BOVIS – BCG (TB)

• Mycobacterium bovis BCG (Tuberculosis) [ATCC 35743]

Test Method Used: Quantitative Tuberculocidal Suspension Test
Organic Soil Load: 5% Horse Serum
Exposure Time: 1 minute at 68°F
Incubation: 21 days at 98.6°F
Results: No growth observed

VIRAL ORGANISM EFFICACY

ENVELOPED VIRUSES

• Herpes Simplex type 2 [ATCC VR-734]
• Human Coronavirus [ATCC VR-740] Strain 229E
• Influenza A virus/Hong Kong Strain [ATCC VR-544]*
• * Pandemic 2009 H1N1 Influenza A virus (Kill claim included)
• Influenza A (H1N1) virus [ATCC VR-98] Strain A/Malaya/302/54
• Vaccinia virus [ATCC VR-1354]

Test Method Used: This test was conducted according to U.S. Environmental Protection Agency guidelines in effect at the time of test for determining the virucidal efficacy of disinfectants intended for use on dry inanimate surfaces.
Organic Soil Load: 5% Fetal Bovine Serum
Exposure Time: 2 minutes at 68°F
Results: Virucidal according to the criteria established by the U.S. Environmental Protection Agency for registration and labeling of a disinfectant product as a virucide.

• Respiratory Syncytial virus (RSV)

Test Method Used: This test was conducted according to U.S. Environmental Protection Agency guidelines in effect at the time of test for determining the virucidal efficacy of disinfectants intended for use on dry inanimate surfaces.
Organic Soil Load: 5% Fetal Bovine Serum
Exposure Time: 1 minute at (68°-77°F)
Results: Virucidal according to the criteria established by the U.S. Environmental Protection Agency for registration and labeling of a disinfectant product as a virucide.

VIRAL ORGANISM EFFICACY

NON-ENVELOPED VIRUSES

• Adenovirus type 5 [ATCC VR-5]
• Rhinovirus [ATCC VR-1110]
• Rotavirus Strain WA

Test Method Used: This test was conducted according to U.S. Environmental Protection Agency guidelines in effect at the time of test for determining the virucidal efficacy of disinfectants intended for use on dry inanimate surfaces.
Organic Soil Load: 5% Fetal Bovine Serum
Exposure Time: 2 minutes at 68°F
Results: Virucidal according to the criteria established by the U.S. Environmental Protection Agency for registration and labeling of a disinfectant product as a virucide.

BLOODBORNE PATHOGENS

• Hepatitis B virus (HBV) 100% duck serum
• Hepatitis C virus (HCV) 5% horse serum

Test Method Used: This test was conducted according to U.S. Environmental Protection Agency guidelines in effect at the time of test for determining the virucidal efficacy of disinfectants intended for use on dry inanimate surfaces.
Organic Soil Load: – Hepatitis B virus (HBV) 100% duck serum Hepatitis C virus
Organic Soil Load: – Hepatitis C virus (HCV) 5% Horse Serum
Exposure Time: 2 minutes at (68°-77°F)
Results: Virucidal against Hepatitis B and Hepatitis C virus aocording to the criteria established by the U.S. Environmental Protection Agency for registration and labeling of a disinfectant product as a virucide

• HIV-1 (AIDS VIRUS)

Test Method Used: This test was conducted according to U.S. Environmental Protection Agency guidelines in effect at the time of test for determining the virucidal efficacy of disinfectants intended for use on dry inanimate surfaces.
Organic Soil Load: – 5% Fetal Bovine Serum
Exposure Time: 30 seconds at (68°F)
Results: Virucidal against Human Immunodeficiency virus type 1 according to the criteria established by the U.S. Environmental Protection Agency for registration and labeling of a disinfectant product as a virucide.

PPATHOGENIC FUNGI EFFICACY

YEAST ORGANISM

• Candida albicans [ATCC 14053]

Test Method Used: Modified AOAC Germicidal Spray Method
Organic Soil Load: 5% Horse Serum
Exposure Time: 2 minutes at 72-74°F
Incubation Time: 2 minutes at 95-98.6°F
Results: No growth observed

TOXICITY

ACUTE ORAL TOXICITY STUDY OF GERMICIDAL DISPOSABLE WIPE
Conclusion: A single-dose of Germicidal Disposable Wipe solution was administered and observed for 14 days. Based on the results of this study, Germicidal Disposable Wipe has an acute oral toxicity LD50 greater than 5 g/kg of body weight.

PRIMARY EYE IRRITATION OF GERMICIDAL DISPOSABLE WIPE
Conclusion: All eye irritation cleared successfully within the respective timed observation period resulting in no permanent eye damage or irritation. In accordance with the OPPTS/OECD Guidelines, Germicidal Disposable Wipe would be classified as Toxicity Category II in unwashed eyes.

ACUTE DERMAL TOXICITY 0F GERMICIDAL DISPOSABLE WIPE
Conclusion: Following the single dermal administration, the subjects were observed for 14 days. Under the conditions of this test, the acute dermal LD50 was found to be greater than 2 g/kg of body weight.

PRIMARY DERMAL IRRITATION 0F GERMICIDAL DISPOSABLE WIPE
Conclusion: The subjects were exposed to the moist towelette with an occlusive wrap for a total of 72 hours. Under the conditions of this study, no dermal irritation was evident at 72 hours.