DIN EN 868-2
Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods
active, Most Current
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| Organization: | DIN |
| Publication Date: | 1 May 2017 |
| Status: | active |
| Page Count: | 27 |
| ICS Code (Sterilized packaging): | 11.080.30 |
scope:
This European Standard specifies test methods and values for materials for sterile barrier systems and/or packaging systems that are intended to maintain sterility of terminally sterilized medical devices to the point of use.
Other than the general requirements as specified in EN ISO 11607-1 and EN ISO 11607-2 this part of EN 868 specifies materials, test methods and values that are specific to the products covered by this European Standard.
While materials specified in 4.2.2.1 to 4.2.2.3 of this part of EN 868 are intended for single use, the materials specified in 4.2.2.4 are intended for reuse.
Document History
DIN EN 868-2
May 1, 2017
Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods
This European Standard specifies test methods and values for materials for sterile barrier systems and/or packaging systems that are intended to maintain sterility of terminally sterilized medical...
August 1, 2015
Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods; German and English version prEN 868-2:2015
A description is not available for this item.
September 1, 2009
Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods
A description is not available for this item.
August 1, 1999
Packaging materials and systems for medical devices which are to be sterilized - Part 2: Sterilization wrap - Requirements and test methods
A description is not available for this item.