This part of YY/T 1293 specifies the requirements for polyurethane foam dressings. This section applies to dressings with a sterile supply of liquid-absorbent layer made of polyurethane foam. This section does not include silver-containing bacteriostatic agents and polyurethane foam dressings for negative pressure drainage.
YY/T 1293.2-2016 Referenced Document
GB/T 14233.1-2008 Test methods for infusion,transfusion,injection equipments for medical use.Part 1:Chemical analysis methods
GB/T 16886.1 Biological evaluation of medical devices—Part 1: Evaluation and testing within a risk management process*， 2022-04-15 Update
GB/T 6682 Water for analytical laboratory use.Specification and test methods
ISO 11607-1:2006 Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems
YY/T 0466.1 Symbols for medical devices used for information provided by manufacturers Part 1: General requirements*， 2023-09-05 Update
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
YY/T 0615.1 Requirements for medical devices to be designated“STERILE”.part 1:Requirements for terminally sterilized medical devices
YY/T 1293.2-2016 history
2022YY/T 1293.2-2022 Contact wound dressings Part 2: Polyurethane foam dressings