Item#: HC500DW Item#: HC100DW Item#: HC50DW Unit Size: 8.38"x 8.38"x 8.75" Unit Size: 5.5"x 7"x 1.5" Unit Size: 5.5"x 7"x 1.5" Unit Weight: 6.31 Lbs Unit Weight: 1.09 lbs Unit Weight: .634 lbs Case Dims: 24"L x 17"W x 9"H Case Dims: 16.5"L x 13.78"W x 7.875"H Case Dims: 16.5"L x 13.78"W x 7.875"H MOQ: (Container) 5400 Units / 900 Cases MOQ: (Container) 47,520 MOQ: (Container) 47,520 Units Per Case 6 Units Per Case 48 Units Per Case 48 Cases per pallet: 45 Cases per pallet: 45 Cases per pallet: 45 Units per pallet: 270 Units per pallet: 2160 Units per pallet: 2160 Pallets per 53' Truckload: 20 Pallets per 53' Truckload: 22 Pallets per 53' Truckload: 22 Units per 53' Truckload: 5400 Units per 53' Truckload: 47520 Units per 53' Truckload: 47520 Pallet Dims: 48 x 40 x 88 Pallet Dims: 48 x 40 x 70 Pallet Dims: 48 x 40 x 70 Case UPC: 10860004463320 Case UPC: 10860004463399 Case UPC: 10860004463337 Unit UPC: 860004463306 Unit UPC: 860004463382 Unit UPC: 860004463313 DUNS #: 11-759-1021 TERMS: 50% Deposit with PO / Balance Due upon Customs Clearance at US Port COUNTRY OF ORIGIN: Israel DELIVERY LEAD TIME: 4 Weeks from Deposit 500-Count 100-Count DISINFECTING & CLEANING WIPES 50-Count
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DISINFECTING & CLEANING WIPES · Multy Purpose Surface Cleaning Wipes Safety Data Sheet Issue date: 6/23/2020 EN (English) 1/6 SECTION 1: Identification of the substance/mixture and
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Item#: HC500DW Item#: HC100DW Item#: HC50DW
Unit Size: 8.38"x 8.38"x 8.75" Unit Size: 5.5"x 7"x 1.5" Unit Size: 5.5"x 7"x 1.5"
Unit Weight: 6.31 Lbs Unit Weight: 1.09 lbs Unit Weight: .634 lbs
Case Dims: 24"L x 17"W x 9"H Case Dims: 16.5"L x 13.78"W x 7.875"H Case Dims: 16.5"L x 13.78"W x 7.875"H
SECTION 6: Accidental release measures 6.1. Personal precautions, protective equipment and emergency procedures
6.1.1. For non-emergency personnel
No additional information available
6.1.2. For emergency responders
No additional information available
6.2. Environmental precautions No additional information available
6.3. Methods and material for containment and cleaning up No additional information available
6.4. Reference to other sections For further information refer to section 13.
SECTION 7: Handling and storage 7.1. Precautions for safe handling Hygiene measures : Do not eat, drink or smoke when using this product. Always wash hands after handling the
product.
7.2. Conditions for safe storage, including any incompatibilities Storage conditions : Keep cool.
7.3. Specific end use(s) No additional information available
SECTION 8: Exposure controls/personal protection 8.1. Control parameters
8.2. Exposure controls No additional information available
SECTION 9: Physical and chemical properties 9.1. Information on basic physical and chemical properties Physical state : Liquid
Appearance : Clear.
Colour : No data available
Odour : No data available
Odour threshold : No data available
pH : 8 - 9.5
Relative evaporation rate (butylacetate=1) : No data available
Melting point : Not applicable
Freezing point : No data available
Boiling point : No data available
Flash point : No data available
Auto-ignition temperature : No data available
Decomposition temperature : No data available
Flammability (solid, gas) : Non flammable.
Vapour pressure : No data available
Relative vapour density at 20 °C : No data available
Relative density : No data available
Density : 0.98 - 0.99 g/cm³
Multy Purpose Surface Cleaning Wipes Safety Data Sheet
6/23/2020 EN (English) 3/6
Solubility : Water: soluble
Log Pow : No data available
Viscosity, kinematic : No data available
Viscosity, dynamic : 1 cP
Explosive properties : Non explosive
Oxidising properties : Non oxidizing
Explosive limits
Storage stability
Corrosion characteristics
: No data available
2 years
Not corrosive
9.2. Other information No additional information available
SECTION 10: Stability and reactivity 10.1. Reactivity The product is non-reactive under normal conditions of use, storage and transport.
10.2. Chemical stability Stable under normal conditions.
10.3. Possibility of hazardous reactions No dangerous reactions known under normal conditions of use.
10.4. Conditions to avoid None under recommended storage and handling conditions (see section 7).
10.5. Incompatible materials No additional information available
10.6. Hazardous decomposition products Under normal conditions of storage and use, hazardous decomposition products should not be produced.
SECTION 11: Toxicological information 11.1. Information on toxicological effects Acute toxicity (oral) : Not classified
Acute toxicity (dermal) : Not classified
Acute toxicity (inhalation) : Not classified
ethanol; ethyl alcohol (64-17-5)
LD50 oral 10470 mg/kg bodyweight
LD50 dermal 15800 mg/kg bodyweight
LC50 inhalation rat (Dust/Mist - mg/l/4h) > 99999 mg/l/4h
Skin corrosion/irritation : Not classified
pH: 8 - 9.5
Serious eye damage/irritation : Not classified
pH: 8 - 9.5
Respiratory or skin sensitisation : Not classified
Germ cell mutagenicity : Not classified
Carcinogenicity : Not classified
Reproductive toxicity : Not classified
STOT-single exposure : Not classified
STOT-repeated exposure : Not classified
Aspiration hazard : Not classified
SECTION 12: Ecological information 12.1. Toxicity Ecology - general : The product is not considered harmful to aquatic organisms nor to cause long-term
adverse effects in the environment.
Hazardous to the aquatic environment, short-term (acute)
: Not classified.
Hazardous to the aquatic environment, long-term
(chronic)
: Not classified
Multy Purpose Surface Cleaning Wipes Safety Data Sheet
- Section 15.1 is related to the raw material and the ingredients, - Raw material is water in 0.1-1 %. This i the water in the raw material not the water in the general formulation,Meaning that in section 15.1 shows the subtitle of the raw material.
CAS. Number Name % by weight Amount gr/l7173-51-5 Didecyl Dimethyl Amonium Chloride 0.2 268424-85-1 Benzalkonium chloride 0.3 364-17-5 ETHANOL 5 5090170-42-6 LAKELAND AMA LF 70 0.5 564-02-8 Tetrasodium EDTA 0.6 668551-12-2 Alcohols, C12-16, ethoxylated 2-15 EO 1.15 11.53586-55-855965-84-9
Determination of Cationic Active Matter content
ISO 2871-1:2010
Surface active agents — Detergents — Determination of cationic-active matter content — Part 1: High-molecular-mass cationic-active matter
THIS STANDARD WAS LAST REVIEWED AND CONFIRMED IN 2017. THEREFORE THIS VERSION REMAINS CURRENT.
Active
Non-active
0.01 0.1MERGAL K14
2020-3788/20 23 00175 1/9
YEDA PHARM
STUDY REPORT
2020-3788/20 23 00175
Disinfectant and Antiseptic Sanitizer Code no. 21060710
SUSPENSION TEST ACCORDING TO EN 1276:2019
(Phase 2 step 1)
Chemical disinfectants and antiseptics Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in food, industrial, domestic and institutional areas – Test method and
SUSPENSION TEST ACCORDING TO EN 1276:2019 Chemical disinfectants and antiseptics – Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in food, industrial, domestic and institutional areas - Test method and requirements (phase 2, step 1)
TEST PRODUCT IDENTIFICATION
PRODUCT NAME : Disinfectant and Antiseptic Sanitizer Code No. 21060710
SUBSTANCES AND THEIR CONCENTRATIONS : Not Provided
APPEARANCE OF THE PRODUCT : Liquid
STORAGE CONDITIONS : Room Temperature, Darkness
LOT : 210607
METHOD : EN 1276:2019
CONTACT TIME : 60 seconds
CONCENTRATION : Undiluted (80%), 50%, 10%.
DILUENT RECOMENTED BY THE MANUFACTURER : Water
CONDITIONS OF TEST : 0.3g/L bovine albumin (Clean conditions)
STUDY SPONSOR : YEDA PHARM
PRODUCT SUPPLIER : YEDA PHARM
RECEIPT DATE : 21/04/2020
STUDY PERIOD : 06/05/2020-08/05/2020
LAB ID : 2020-3788/20 23 00175
SCOPE
This document specifies a test method and the minimum requirements for bactericidal activity of chemical disinfectant and antiseptic products that form a homogeneous, physically stable preparation when diluted with hard water or - in the case of ready-to-use products - with water. Products can only be tested at a concentration of 80 % or less, as some dilution is always produced by adding the test organisms and interfering substance.
This document applies to products that are used in food, industrial, domestic and institutional areas
excluding areas and situations where disinfection is medically indicated and excluding products used on living tissues except those for hand hygiene in the above considered areas
PRINCIPLE
A sample of the product as delivered and/or diluted with hard water (or water for ready-to-use products with the exception of handwash products whose first dilution is done in hard water is added to a test suspension of bacteria in a solution of an interfering substance. The mixture is maintained at the chosen test temperature for the adopted contact time. At the end of this contact time, an aliquot is taken, and the bactericidal and/or the bacteriostatic activity in this portion is immediately neutralized or suppressed by a validated method. The method of choice is dilution-neutralization. If a suitable neutralizer cannot be found, membrane filtration is used. The numbers of surviving bacteria in each sample are determined and the reduction is calculated.
The test is performed using Pseudomonas aeruginosa, Escherichia coli, Staphylococcus aureus and Enterococcus hirae as test organisms. For temperatures ≥ 40 °C only Enterococcus faecium shall be used. For testing of hand hygiene products, Pseudomonas aeruginosa, Escherichia coli K12, Staphylococcus aureus and Enterococcus hirae are used as test organisms.
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TEST CONDITIONS
1. The following procedure was performed in water bath at 20 °C
2. The test product was tested at 60 seconds contact time
3. A final concentration of 0.3g/L bovine albumin was used for testing (clean conditions)
6. According to EN 1276, products shall be tested at a minimum of three different
concentrations to include one concentration in the active range and one concentration in
the non-active range. In this case the product was tested: Undiluted, 50% 10%.
TEST ORGANISMS
Pseudomonas aeruginosa NCIMB 10421
Staphylococcus aureus ATCC 6538
Escherichia coli NCIMB 8879
Enterococcus hirae NCIMB 8192
BACTERICIDAL ACTIVITY FOR GENERAL PURPOSES
The product shall be deemed to have passed the EN 1276 standard if it demonstrates in a valid test at least a 5 lg reduction, under the suitable test conditions for general purpose defined by this standard when the test organisms are Pseudomonas aeruginosa, Escherichia coli, Staphylococcus aureus and Enterococcus hirae (E. faecium when the test temperature is ≥ 40 °C).
ASSAY ACCEPTANCE CRITERIA
1. Test Suspension (N) is between 1.5 to 5.0 X 108 CFU per mL (8.17≤log N≤8.70)
2. No (N/10) is between 1.5 to 5.0 X 107 CFU per mL (7.17≤log No≤7.70)
3. Validation Suspension=Nν is between 3.0 x 102 and 1.6 x 103.
4. Nvo (Nv/10) is between 30 and 160
5. Na is the number of survivors (cells) per ml in the test mixture at the end of contact time.
6. R (log reduction) = No - Na
7. Average recovery values for the experimental conditions control (Α) were equal to or
greater than 0.5 times the Validation Suspension (Nνo)
8. Average recovery values for the Neutralizer control (Β) were equal to or greater than 0.5
times the Validation Suspension (Nνo)
9. Average recovery values for the Method Validation control (C) were equal to or greater than
0.5 times the Validation Suspension (Nνo)
10. Control of weighted mean counts. Quotient is not lower than 5 and not higher than 15
ARCHIVING
The laboratory book which contains all the information (raw data and results) regarding the study and the study reports are kept in the laboratory archives for 5 years.
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TEST RESULTS FOR Pseudomonas aeruginosa (BACTERICIDAL SUSPENSION TEST)
Test suspensionTest - suspension(N and Nο)
N Vc1 Vc2 x mean
10-6
10-7
log N 8.30
No (N/10)
log No 7.30
7,17 < = logNo < = 7,70 Yes
Validation and controls
Validation suspension
(Nνο)
VC 1 52 VC 1 49 VC 1 49 x mean VC 1 55
VC 2 54 53 VC 2 51 VC 2 47 48 VC 2 52
30<x mean of Nνo < 160? x mean of A is > 0,5*x mean of Nνo? x mean of B is > 0,5*x mean of Nνo or NVB/1000? x mean of C is > 0,5*x mean of Nνo?
Yes Yes Yes Yes
Test Results
10 0 0 0 0 010 -1 0 0 0 0
100
0 0 0 0
10-1
0 0 0 0
100
> 330 > 330
10-1
> 330 > 330
Undiluted
(80%)
x mean x mean x mean
Experimental conditions (A)
53.5
2.02E+08
2.02E+07
Method validation (C)
Product conc.: Neutralizer control (B)
17 23
198 206
Criteria
≥ 5
≥ 5
≥ 5
Result
PASS TEST
PASS TEST
FAILS TEST
7.30
7.30
> 5.16
7.30
>
Product concentration (%)
Undiluted (80%)
50%
10%
Contact time Dilution step
60 sec
60 sec 14
log Na log No
log
Reduction
(No-Na)
> 3300 4.52
< 5.16
< 2.79
<
<140
> 33000
Vc 2Average of Vc1
and Vc2
50
>60 sec
Na= average x10
2.15140<14<
Vc 1
2.15<
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TEST RESULTS FOR Staphylococcus aureus (BACTERICIDAL SUSPENSION TEST)
Test suspensionTest - suspension(N and Nο)
N Vc1 Vc2 x mean
10-6
10-7
log N 8.26
No (N/10)
log No 7.26
7,17 < = logNo < = 7,70 Yes
Validation and controls
Validation suspension
(Nνο)
VC 1 43 VC 1 47 VC 1 51 x mean VC 1 42
VC 2 46 44.5 VC 2 42 VC 2 48 49.5 VC 2 46
30<x mean of Nνo < 160? x mean of A is > 0,5*x mean of Nνo? x mean of B is > 0,5*x mean of Nνo or NVB/1000? x mean of C is > 0,5*x mean of Nνo?
Experimental conditions (A) Neutralizer control (B)Method validation (C)
Product conc.:
Undiluted
(80%)
1.98E+07
21 19
1.98E+08
192 204
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CONCLUSION
TEST SUBSTANCE IDENTIFICATION
PRODUCT NAME : Disinfectant and Antiseptic Sanitizer Code No. 21060710
SUBSTANCES AND THEIR CONCENTRATIONS : Not Provided
APPEARANCE OF THE PRODUCT : Liquid
STORAGE CONDITIONS : Room Temperature, Darkness
LOT : 210607
METHOD : EN 1276:2019
CONTACT TIME : 60 seconds
CONCENTRATION : Undiluted (80%), 50%, 10%.
DILUENT RECOMENTED BY THE MANUFACTURER : Water
CONDITIONS OF TEST : 0.3g/L bovine albumin (clean conditions)
STUDY SPONSOR : YEDA PHARM
PRODUCT SUPPLIER : YEDA PHARM
RECEIPT DATE : 21/04/2020
STUDY PERIOD : 06/05/2020-08/05/2020
LAB ID : 2020-3788/20 23 00175
METHODOLOGY ABSTRACT
A test suspension of bacteria (P. aeruginosa, S. aureus, E. coli & E. hirae) is tested against a product test solution at three different concentrations with the presence of interfering substance. The mixture is maintained at 20°C ±1°C for 5 minutes. At the end of this contact time, an aliquot is taken, and the bactericidal activity in this portion is immediately neutralized or suppressed. The numbers of surviving flora are determined and the log reduction is calculated.
RESULT
The product under test: “Disinfectant and Antiseptic Sanitizer Code No. 21060710” demonstrated bactericidal activity according to EN 1276:2019 (≥ 5 log reduction), under clean conditions, for 60
seconds contact time, at 20 1 °C, when tested at product concentration: Undiluted (80%) using as test organisms the reference strains: P. aeruginosa, S. aureus, E. coli & E. hirae. For the QACS Ltd Laboratory,
Signature date: 14/05/2020 Lagiopoulos Giorgos Agronomist-Food Technologist M.Sc. Study Manager
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STUDY SUMMARY / ABSTRACT
SUSPENSION TEST ACCORDING TO EN 1276:2019 Chemical disinfectants and antiseptics – Basic Bactericidal activity Test methods and requirements (Phase 2 Step 1)
PRODUCT NAME : Disinfectant and Antiseptic Sanitizer Code
No. 21060710
SUBSTANCES AND THEIR CONCENTRATIONS : Not Provided
APPEARANCE OF THE PRODUCT : Liquid
STORAGE CONDITIONS : Room Temperature, Darkness
LOT : 210607
METHOD : EN 1276:2019
CONTACT TIME : 60 seconds
CONCENTRATION : Undiluted (80%), 50%, 10%.
DILUENT RECOMENTED BY THE MANUFACTURER : Water
CONDITIONS OF TEST : 0.3g/L bovine albumin (clean conditions)
STUDY SPONSOR : YEDA PHARM
PRODUCT SUPPLIER : YEDA PHARM
RECEIPT DATE : 21/04/2020
STUDY PERIOD : 06/05/2020-08/05/2020
LAB ID : 2020-3788/20 23 00175
TEST MICROORGANISMS
Pseudomonas aeruginosa NCIMB 10421
Staphylococcus aureus ATCC 6538
Escherichia coli NCIMB 8879
Enterococcus hirae NCIMB 8192
RESULT
The product under test: “Disinfectant and Antiseptic Sanitizer Code No. 21060710” demonstrated bactericidal activity according to EN 1276:2019 (≥ 5 log reduction), under clean conditions, for 60
seconds contact time, at 20 1 °C, when tested at product concentration:
Undiluted (80%) using as test organisms the reference strains: P. aeruginosa, S. aureus, E. coli & E. hirae
Results refer to the sample as received and analyzed on the period specified above.
The test report shall not be reproduced except in full, without written approval of the laboratory.
The samples will be stored by the laboratory during 1 month from the end test date.
The study report and raw data will be stored by the laboratory for 5 years.