AnshLiteTM PAPP-A CLIA

Ansh Labs

Revision date : 2016-06-23

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GHS07
Health risk rating 4
Safety risk rating 1
Environmental risk rating 1

Note: Ingredients listed on restricted chemical lists

EC/CAS

26628-22-8

Name of the chemical

Sodium Azide

Concentration

N/A

EC/CAS

55965-84-9

Name of the chemical

Mixture of 5-chloro-2-methyl-2H- isothiazol-3-one (EINECS 247-500-7) and 2-methyl-2H-isothiazol-3-one (EINECS 220-239-6)

Concentration

N/A

EC/CAS

220-239-6

Name of the chemical

Mixture of 5-Chloro-2-methyl-isothiazol-3(2H)-one and 2-methylisothiazol-3(2H)-one 2-Methyl-2H-isothiazol-3-one

Concentration

N/A

EC/CAS

247-500-7

Name of the chemical

Mixture of 5-Chloro-2-methyl-isothiazol-3(2H)-one and 2-methylisothiazol-3(2H)-one

Concentration

N/A

General Information

Revision date

2016-06-23

Product name

AnshLiteTM PAPP-A CLIA

Manufacturer Name

EC Representative

Icons in SDS

Company Information

company name

Ansh Labs

e-mail address of the competent person responsible for the Safety Data Sheet

techsupport@anshlabs.com

GHS Information

Signal word

Warning

Hazard Codes

Hazard statements (CLP)

H317, H319

Hazard statements

Code

Statements

H317

May cause an allergic skin reaction

Section 2

2.1 Classification of the substance or mixture

None of the material of this product may be classified as or mixture: dangerous according to EC Directives 1999/45/EC, 67/548/EEC and 1272/2008/EC due to the low concentration of hazardous ingredients.

2.2 Label elements

Pro-clean 400: R23/24/25: Harmful if inhaled, in contact with skin and if swallowed H317 May cause an allergic skin reaction H319 Causes serious eye irritation Hydrogen Peroxide: H335.May cause respiratory irritation

2.3 Other hazards

Not applicable. Note: The Calibrators and Controls are formulated with a buffer base, animal serum and human serum. The human serums are tested by a CE licensed method and found to be non-reactive for HIV-1, HIV-2, Hepatitis B surface antigen and HCV. Because no test method can offer absolute assurance that these agents are absent, reagents should be handled at the Biosafety Level 2, as recommended for any potentially infectious human blood product. Bovine products ( BSA ) have been derived from US origin and processed in USDA licensed facilities, and are free from known infections, however, it should be considered that no available test method can offer complete assurance of eliminating potential biohazardous risk. The antibodies are from monoclonal origin and are free from human or animal source

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