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This international standard specifies requirements and test methods for the design and performance of packaging systems used for transporting medical devices provided non-sterile to the point of use.
Product designed and developed to be shipped non-sterile from the manufacturer is covered by the requirements in this document. It does not apply to packaging for terminally sterilized medical devices which are covered by ISO 11607-1/-2.
It does not apply to packaging materials and/or systems used to contain a contaminated medical device during transportation of the item to the site of reprocessing or disposal.
It does not apply to the maintenance of a certain microbiological state which would require integrity and microbial barrier properties.
[Note: Some changes have been made to the Scope in response to the comments received in the first NWI ballot for ISO/NP 22246.]
Reģistrācijas numurs (WIID)
89180
Darbības sfēra
This international standard specifies requirements and test methods for the design and performance of packaging systems used for transporting medical devices provided non-sterile to the point of use.
Product designed and developed to be shipped non-sterile from the manufacturer is covered by the requirements in this document. It does not apply to packaging for terminally sterilized medical devices which are covered by ISO 11607-1/-2.
It does not apply to packaging materials and/or systems used to contain a contaminated medical device during transportation of the item to the site of reprocessing or disposal.
It does not apply to the maintenance of a certain microbiological state which would require integrity and microbial barrier properties.
[Note: Some changes have been made to the Scope in response to the comments received in the first NWI ballot for ISO/NP 22246.]
