AnshCheck 1T-2T Maternal Screening Bi-Level

Ansh Labs

Revision date : 2019-02-26

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Health risk rating 1
Safety risk rating 1
Environmental risk rating 1

Note: Ingredients listed on restricted chemical lists

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

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

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

General Information

Revision date

2019-02-26

Product name

AnshCheck 1T-2T Maternal Screening Bi-Level

CAS No.

55965-84-9

1.2.1 Relevant identified uses

Intended for use as assay quality controls to monitor the

1.2.2. Uses advised against

precision and reproducibility of laboratory testing methods for the determination of AFP, Inhibin A, free beta hCG, Estriol, PAPP-A

Manufacturer Name

EC Representative

Emergency telephone

In the event of a medical emergency, please dial 911

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

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 REACH and EC Directive 1272/2008/EC due to the low concentration of hazardous ingredients.

2.2 Label elements

Not applicable.

2.3 Other hazards

Not applicable. Note: this product is intended for laboratory use by professional uses only. Use appropriate personal protective equipment while working with the reagents provided. The Controls are formulated with Human serum and saline solution. The human serums are tested by a CE/FDA licensed method and found to be non-reactive for HIV-1, HIV-2, Hepatitis B, Syphilis 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.

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