YY 0167-2005 Replaced Industry standards-Medicine

YY 0167-2005 Non-absorbable surglcal suture

YY 0167-2005 Non-absorbable surglcal suture

Publish Date: 2005-07-18 Implement Date: 2006-06-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: YY 0167-2005

Standard Type: Industry standards

Standard Status: Replaced

is_force_gb: no

CCS Name: Generally, it refers to microsurgical instruments

ICS Name: Surgical instruments and materials

Publish Date: 2005-07-18

Implement Date: 2006-06-01

Pages: 10 pages

Scope

This standard specifies the classification, requirements, test methods, inspection rules, marking, user's manual, packaging, transportation, and storage of non-absorbable surgical sutures. This standard applies to non-absorbable surgical sutures (hereinafter referred to as sutures) used for suturing and ligating human tissues during medical procedures.

Development Information

Word Count: 16 Thousand words Pages: 10 pages

Replace the following standards

YY 0167-1998 Non-absorbable Surgical Suture

Superseded by the following standards

YY 0167-2020 Non-absorbable surgical suture

Referenced Standards

GB/T 9737-198 GB/T 14233.1-1998 Infusion,transfusion,injection equipment for medical use—Part 1:Chemical analysis methods GB/T 16175-1996 Organic silicon material for medical use—Biological evaluation test methods GB/T 16886.3-1997 Biological evaluation of medical devices—Part 3:Tests for genotoxicity, carcinogenicity and reproductive toxicity GB/T 16886.10-2005 Biological evaluation of medical devices—Part 10:Tests for irritation and delayed-type hypersensitivity YY 0466-2003 Medical devices—Symbols to be used with medical device labels,labelling and information to be supplied Y 0043 中华人民共和国药典(2000年版) GB/T 14436-1993 General principles of industrial product guarantee documents GB/T 16886.1-2001 Biological evaluation of medical devices—Part 1:Evaluation and testing GB/T 16886.1-2011 Biological evaluation of medical devices—Part 1:Evaluation and testing within a risk management process GB/T 16886.1-2022 Biological evaluation of medical devices—Part 1:Evaluation and testing within a risk management process

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