YY/T 1293.2-2016 Replaced Industry standards-Medicine

YY/T 1293.2-2016 Contacting wound dressing—Part 2:Polyurethane foam dressing

YY/T 1293.2-2016 Contacting wound dressing—Part 2:Polyurethane foam dressing

Publish Date: 2016-03-23 Implement Date: 2017-01-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: YY/T 1293.2-2016
Standard Type: Industry standards
Standard Status: Replaced
is_force_gb: no
CCS Name: Medical hygiene products
ICS Name: Medical materials
Publish Date: 2016-03-23
Implement Date: 2017-01-01
Pages: 8 pages

Scope

This part of YY/T 1293 specifies the requirements for polyurethane foam dressings.
This part applies to dressings with a liquid-absorbent layer made of polyurethane foam that are supplied in a sterile form.
This part does not include polyurethane foam dressings containing antibacterial agents such as silver and those used for negative pressure drainage.

Development Information

Word Count: 14 Thousand words Pages: 8 pages

Same series standard

Superseded by the following standards

Referenced Standards

GB/T 14233.1-2008 Test methods for infusion,transfusion,injection equipments for medical use—Part 1:Chemical analysis methods YY/T 0471.1-2004 Test methods for primary wound dressing—Part 1:Aspects of absorbency YY/T 0471.2-2004 Test methods for primary wound dressings—Part 2:Moisture vapour transmission rate of permeable film dressings YY/T 0471.3-2004 Test methods for primary wound dressings—Part 3:Waterproofness YY/T 0471.5-2004 Test methods for primary wound dressing—Part 5:Bacterial barrier properties ISO 11607-1:2006 GB/T 6682-1992 Water for analytical laboratory use—Specification and test methods GB/T 6682-2008 Water for analytical laboratory use—Specification and test methods 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 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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