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Showing 1 - 12 from 15 Standards Found 15 Standards
OS GSO ASTM F1980:2024
ASTM F1980:21 
Omani Standard
Standard Guide for Accelerated Aging of Sterile Barrier Systems and Medical Devices
GSO ASTM F1980:2024
ASTM F1980:21 
Gulf Standard
Standard Guide for Accelerated Aging of Sterile Barrier Systems and Medical Devices
ISO 11607-2:2019/Amd 1:2023
 
Amendment to International Standard
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes — Amendment 1: Application of risk management
ISO 11607-1:2019/Amd 1:2023
 
Amendment to International Standard
Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems — Amendment 1: Application of risk management
GSO ISO 11607-2:2021
ISO 11607-2:2019 
Gulf Standard
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes
OS GSO ISO 11607-1:2021
ISO 11607-1:2019 
Omani Standard
Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems
GSO ISO 11607-1:2021
ISO 11607-1:2019 
Gulf Standard
Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems
OS GSO ISO 11607-2:2021
ISO 11607-2:2019 
Omani Standard
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes
ISO/TS 16775:2021
 
International Standard
Packaging for terminally sterilized medical devices — Guidance on the application of ISO 11607-1 and ISO 11607-2
ISO 21882:2019
 
International Standard
Sterile packaged ready for filling glass vials
ISO 11607-2:2019
 
International Standard
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes
ISO 11607-1:2019
 
International Standard
Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems