YY/T 1231-2014
Active
Industry standards-Medicine
YY/T 1231-2014 Creatinine test reagent kit(Method of sarcosine oxidase)
YY/T 1231-2014 Creatinine test reagent kit(Method of sarcosine oxidase)
Basic Information
Standard Code:
YY/T 1231-2014
Standard Type:
Industry standards
Standard Status:
Active
is_force_gb:
no
CCS Name:
Medical laboratory equipment
ICS Name:
Laboratory medicine
Publish Date:
2014-06-17
Implement Date:
2015-07-01
Pages:
10 pages
Scope
This standard specifies the technical requirements, test methods, labels, user manuals, packaging, transportation, and storage for creatinine assay reagents (kits) using the sucrase oxidase method.
This standard applies to creatinine assay reagents (kits) used to quantitatively detect creatinine concentrations in serum, plasma, and urine using the sucrase oxidase method, including manual reagents and reagents used on semi-automatic and fully automatic biochemical analyzers.
This standard does not apply to creatinine assay reagents (kits) using the picric acid method.
This standard does not apply to dry-type creatinine assay reagents (kits).
Development Information
Referenced Standards
GB/T 21415-2008 In vitro diagnostic medical devices—Measurement of quantities in biological samples—Metrological traceability of values assigned to calibrators and control materials
GB 3100-1993 SI units and recommendations for the use of their multiples and of certain other units
YY/T 0316-2003 Medical devices—Application of risk management to medical devices
YY/T 0316-2008 Medical devices—Application of risk management to medical devices
YY/T 0316-2016 Medical devices—Application of risk management to medical devices
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
YY/T 0316-2000 YY/T 0316-2000 Medical devices - Risk analysis - Part 1: Application of risk analysis
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