In-Vitro Diagnostic (IVD) Device-Automated Clinical Chemistry Analyzer - Part 2 Dry Chemistry Analyzer

Available format(s)

Hardcopy

Language(s)

English

Published date

01-01-2023

Publisher

Bureau of Indian Standards

This part of Indian standard provides basic requirements and standard test procedures for performance testing of In-Vitro diagnostic (IVD) instruments - Automated clinical chemistry Analyzers also known as Biochemistry Analyzers including random access, high throughput fully automated clinical chemistry analysers for dry chemistry analyzer only.

Committee	MHD 19
DocumentType	Standard
Pages	0
ProductNote	This standard also refers to IS/IEC 61010-1 : 2010
PublisherName	Bureau of Indian Standards
Status	Current

IS 17784 : Part 2 : 2023

Electrical Equipment for Measurement, Control and Laboratory Use-EMC Requirements - Part 2 Particular Requirements for In-vitro Diagnostic (IVD) Medical Equipment (IEC 61326-2-6 : 2020, MOD)

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IS 17717 : Part 2 : 2023

In-Vitro Diagnostic (IVD) Device-Automated Clinical Chemistry Analyzer - Part 2 Dry Chemistry Analyzer

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