AENOR UNE-EN ISO 11607-2:2020

Description
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)
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Description
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)
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UNE-EN ISO 11607-2:2020 -  - AENOR
MadrId, Spain
UNE-EN ISO 11607-2:2020
UNE-EN ISO 11607-2:2020
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)

Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)

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Technical Specifications

  AENOR
Product Category Standards and Technical Documents
Product Name UNE-EN ISO 11607-2:2020
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