Standard Guide for Accelerated Aging of Sterile Medical Device Packages
This product is not for sale, please contact us for more information
Packaging materials and systems for medical devices which are to be sterilized Re-usable sterilization containers steam sterilizers conforming EN 285. Requirements test methods
€165.00
Packaging materials and systems for medical devices which are to be sterilized Adhesive coated paper the manufacture of heat sealable packs use sterilization by ethylene oxide or irradiation. Requirements test methods
Packaging materials and systems for medical devices which are to be sterilized Paper the manufacture of packs use sterilization by ethylene oxide or irradiation. Requirements test methods
Packaging materials and systems for medical devices which are to be sterilized Paper bags. Requirements test methods
Packaging materials and systems for medical devices which are to be sterilized Paper use in the manufacture of paper bags (specified EN 868-4) pouches reels 868-5). Requirements test methods
Packaging materials and systems for medical devices which are to be sterilized Sterilization wrap. Requirements test methods
Packaging materials and systems for medical devices which are to be sterilized General requirements test methods
€193.00
Packaging materials and systems for medical devices which are to be sterilized Uncoated nonwoven of polyolefines use in the manufacture heat sealable pouches, reels lids. Requirements test methods
Packaging materials and systems for medical devices which are to be sterilized Adhesive coated nonwoven of polyolefines use in the manufacture heat sealable pouches, reels lids. Requirements test methods
BS EN 868-9 Packaging for terminally sterilized medical devices Part 9: Uncoated nonwoven materials of polyolefines - Requirements and test methods
€23.00
BS EN 868-8 Packaging for terminally sterilized medical devices Part 8: Re-usable sterilization containers large steam sterilizers. Requirements and test methods
Standard Guide for Accelerated Aging of Sterile Barrier Systems for Medical Devices
Standard Test Method for Verifying Nonporous Flexible Barrier Material Resistance to the Passage of Air
