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What sterilization and storage requirements must medical non-woven fabrics meet? 2021-02-16

The quality of medical non-woven fabrics must meet the national standards. This is a mandatory requirement. However, since there are still companies in the non-woven fabric industry that use inferior raw materials to save costs, the quality inspection and Supervision is an indispensable measure to ensure the quality of medical non-woven fabrics. So what requirements must medical non-woven fabrics meet?


1. Non-woven packaging materials should meet the requirements of "GB/T19663.1-2015 Packaging for Terminally Sterilized Medical Devices":

Microbial barrier, water resistance, compatibility with human tissues, air permeability, salt water resistance, surface absorption, toxicology test, maximum equivalent pore size, drape, tensile strength, wet tensile strength and burst resistance They are in compliance with relevant national regulations and should be used once.


2. Storage environment requirements

The storage requirements of medical non-woven fabrics meet the requirements of YY/T0698.2-2009.


That is, the temperature of the inspection, packaging and sterilization area is 20℃-23℃, the relative humidity is 30%-60%, and the mechanical ventilation is 10 times in 1 hour. The cotton dressing packing room must be separated from the equipment packing room to avoid cotton dust pollution of the equipment and Packaging materials such as woven cloth.


For more medical non-woven fabric information, please contact us.Email: long@guideco.cn


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