YY/T 0456.1-2003
Replaced
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)
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
Referenced Standards
YY/T 0466.1-2009 Medical devices—Symbols to be used with medical device labels, labelling and information to be supplied—Part 1:General requirements
YY/T 0466.1-2016 Medical devices—Symbols to be used with medical device labels,labelling and information to be supplied—Part 1:General requirements
YY/T 0466.1-2023 Medical devices—Symbols to be used with information to be supplied by the manufacturer—Part 1:General requirements
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