GB 12264-1990
Replaced
YY/T 1682-2019
Active
Industry standards-Medicine
YY/T 1682-2019 Ureaplasma spp./Mycoplasma hominis culture and antimicrobial susceptibility testing kit
YY/T 1682-2019 Ureaplasma spp./Mycoplasma hominis culture and antimicrobial susceptibility testing kit
Basic Information
Standard Code:
YY/T 1682-2019
Standard Type:
Industry standards
Standard Status:
Active
is_force_gb:
no
CCS Name:
Medical optical instruments and equipment, and endoscopes
ICS Name:
Surgical implants, prostheses, and orthoses
Publish Date:
2019-10-23
Implement Date:
2021-10-01
Pages:
10 pages
Scope
This standard specifies the requirements, test methods, labels, user manuals, packaging, transportation, and storage for Ureaplasma/Mycoplasma hominis culture and drug sensitivity detection kits.
This standard only applies to culture and drug sensitivity detection kits (including separate culture identification kits, hereinafter referred to as "kits") based on the color change caused by biochemical reactions during the culture process of Ureaplasma spp. and Mycoplasma hominis (MH).
The drug sensitivity compliance rate test in this standard is not applicable to separate culture kits.
Development Information
Referenced Standards
中华人民共和国药典
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
Related Standards
GB 12279-1990
Replaced
GB 12279-1990 Cardiac valve prostheses general technical specification
GB 12417-1990
Replaced
GB 12417-1990 The general technological conditions of surgical metal implant
GB/T 13461-1992
Replaced
GB/T 13461-1992 Synthetic resin blow knee prostheses
GB/T 14191-1993
Replaced
GB/T 14191-1993 Terminology for prosthetics and orthotics
GB 14722-1993
Replaced