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          Paper bags - bags of quality medical equipment technical requirements

          1 , including the material must be an effective barrier to microorganisms / bacteria ASTM F-1608.
          2 , must adapt to the sterilization commitment ISO11134 \ ISO11135 \ ISO11137.
          3 , to maintain the sterility of the product . Packaging is not to have the opportunity to be intrusive air pollution, fiber breakage , dust and other foreign matter , microorganisms (ASTM D-2019). Therefore , the need to ensure that the packaging : - including materials without damage ; seal integrity, peel strength (ASTM F88) appropriate, no penetration (ASTM: 1998), no blasting (ASTM F-1150 / ASTM F-2054), stripped clean ( EN868-5).
          4 , comprises a material or packaging to be appropriate to be subsequent processing; material is required when the maximum degree of reduction of the shedding of particles , such as fibers, flakes , off ink and dust . (ASTM D-2019).
          5 , after opening , there should have been obvious traces show opened ; packaged unsealed mouth open , there should not be any re- sealing property . ( Prevention of contaminated packaging and re- open closed ) .
          6 , should identify the open position and orientation ; should be easily opened, and the opening position should facilitate users to play open (EN980).
          7 , must be able to identify other products ( print marks should be consistent with the medical device laws and regulations, including the materials side of the transparent material , you can see the inside of the product ) EN980.
          | Updated:2014.04.16    Source:    Clicks:30288

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