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ISO 11607-2:2006

Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes

Standard Details

ISO 11607-2:2006 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing, and assembly of preformed sterile barrier systems, sterile barrier systems and packaging systems.

ISO 11607-2:2006 is applicable to industry, to health care facilities, and wherever medical devices are packaged and sterilized.

ISO 11607-2:2006 does not cover all requirements for packaging medical devices that are manufactured aseptically. Additional requirements may also be necessary for drug/device combinations.

General Information

Status : WITHDRAWN
Standard Type: Main
Document No: ISO 11607-2:2006
Document Year: 2006
Pages: 11
Edition: 1
  • Section Volume:
  • ISO/TC 198. Sterilization of health care products

Life Cycle

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WITHDRAWN
ISO 11607-2:2006
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