YY/T 1627-2018 Active Industry standards-Medicine

YY/T 1627-2018 General requirements of acute adhesive wound dressing and woundplast

YY/T 1627-2018 General requirements of acute adhesive wound dressing and woundplast

Publish Date: 2018-11-07 Implement Date: 2019-11-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: YY/T 1627-2018
Standard Type: Industry standards
Standard Status: Active
is_force_gb: no
CCS Name: Medical hygiene products
ICS Name: Medical materials
Publish Date: 2018-11-07
Implement Date: 2019-11-01
Pages: 13 pages

Scope

This standard specifies the general requirements for dressings and wound dressings used for acute wounds on the body surface, such as surgical incisions, puncture wounds, or mechanical wounds.
This standard applies to dressings and wound dressings whose main structural features consist of an adhesive layer, an absorbent pad, and a release layer.
This standard does not apply to hydrocolloid dressings and wound dressings for acute wounds.
This standard does not apply to dressings and wound dressings that contain specific substances with antibacterial and anti-inflammatory effects (such as silver and chitosan).

Development Information

Word Count: 22 Thousand words Pages: 13 pages

Referenced Standards

GB/T 14233.1-2008 Test methods for infusion,transfusion,injection equipments for medical use—Part 1:Chemical analysis methods YY/T 0148-2006 Medical adhesive bandages—General requirements YY/T 0471.1-2004 Test methods for primary wound dressing—Part 1:Aspects of absorbency YY/T 0471.3-2004 Test methods for primary wound dressings—Part 3:Waterproofness YY/T 0471.4-2004 Test methods for primary wound dressing—Part 4:Conformability 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 GB/T 19633.1-2015 Packaging for terminally sterilized medical devices—Part 1:Requirements for materials, sterile barrier systems and packaging systems GB/T 19633.1-2024 Packaging for terminally sterilized medical devices—Part 1:Requirements for materials,sterile barrier systems and packaging systems 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 0615.1-2007 Requirements for medical devices to be designated "STERILE"—Part 1:Requirements for terminally sterilized medical devices

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