YY/T 1220-2013 Active Industry standards-Medicine

YY/T 1220-2013 (Creatine kinase isoenzyme MB)(CK-MB) diagnostic kit(Colloid gold method)

YY/T 1220-2013 (Creatine kinase isoenzyme MB)(CK-MB) diagnostic kit(Colloid gold method)

Publish Date: 2013-10-21 Implement Date: 2014-10-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: YY/T 1220-2013
Standard Type: Industry standards
Standard Status: Active
is_force_gb: no
CCS Name: Medical laboratory equipment
ICS Name: Laboratory medicine
Publish Date: 2013-10-21
Implement Date: 2014-10-01
Pages: 7 pages

Scope

This standard specifies the terms and definitions, requirements, test methods, inspection and judgment, marking, labels, and user manuals, packaging, transportation, and storage for creatine kinase isoenzyme (CK-MB) diagnostic reagents (kits) (colloidal gold method).
This standard applies to creatine kinase isoenzyme (CK-MB) diagnostic reagents (kits) (colloidal gold method). The reagent is used for the in vitro qualitative detection of creatine kinase isoenzyme (CK-MB) activity in human serum or plasma.

Development Information

Word Count: 12 Thousand words Pages: 7 pages

Referenced Standards

Related Standards

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