YY/T 1596-2017
Active
Industry standards-Medicine
YY/T 1596-2017 Influenza A virus nucleic acid detection kit(fluorescent PCR)
YY/T 1596-2017 Influenza A virus nucleic acid detection kit(fluorescent PCR)
Basic Information
Standard Code:
YY/T 1596-2017
Standard Type:
Industry standards
Standard Status:
Active
is_force_gb:
no
CCS Name:
Medical laboratory equipment
ICS Name:
Laboratory medicine
Publish Date:
2017-12-05
Implement Date:
2018-12-01
Pages:
7 pages
Scope
This standard specifies the terms and definitions, requirements, test methods, labels and instructions, as well as packaging, transportation, and storage for the influenza A virus nucleic acid detection kits (fluorescence PCR method) (hereinafter referred to as "kits").
This standard applies to kits that use the fluorescence PCR method to qualitatively detect the influenza A virus nucleic acid in human nasal and throat swabs or other respiratory secretion samples.
This standard does not apply to kits that use the isothermal amplification method to qualitatively detect the influenza A virus nucleic acid in human nasal and throat swabs or other respiratory secretion samples.
Development Information
Referenced Standards
GB/T 191-2000 Packaging—Pictorial marking for handling of goods
GB/T 191-2008 Packaging—Pictorial marking for handling of goods
GB/T 29791.2-2013 In vitro diagnostic medical devices—Information supplied by the manufacturer (labelling)—Part 2:In vitro diagnostic reagents for professional use
GB/T 191-2025 Graphical symbols marking for handling and storage of packages
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