GB/T 29791.1-2013 Active National standards

GB/T 29791.1-2013 In vitro diagnostic medical devices—Information supplied by the manufacturer(labelling)—Part 1:Terms,definitions and general requirements

GB/T 29791.1-2013 In vitro diagnostic medical devices—Information supplied by the manufacturer(labelling)—Part 1:Terms,definitions and general requirements

Publish Date: 2013-10-10 Implement Date: 2014-02-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: GB/T 29791.1-2013

Standard Type: National standards

Standard Status: Active

is_force_gb: no

CCS Name: Medical laboratory equipment

ICS Name: Laboratory medicine

Publish Date: 2013-10-10

Implement Date: 2014-02-01

Pages: 41 pages

Scope

This part of GB/T 29791 defines the concepts of information provided by manufacturers of in vitro diagnostic medical devices, establishes general principles, and stipulates basic requirements.

Development Information

Word Count: 72 Thousand words Pages: 41 pages

Same series standard

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 29791.3-2013 In vitro diagnostic medical devices—Information supplied by the manufacturer(labelling)—Part 3:In vitro diagnostic instruments for professional use GB/T 29791.4-2013 In vitro diagnostic medical devices—Information supplied by the manufacturer (labelling)—Part 4:In vitro diagnostic reagents for selftesting GB/T 29791.5-2013 In vitro diagnostic medical devices—Information supplied by the manufacturer (labelling)—Part 5:In vitro diagnostic instruments for selftesting

Referenced Standards

ISO 1000 ISO 13485 ISO 14971 ISO 15223-1 IEC 62366 EN 980

Adopt standards

ISO 18113-1:2009

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