Sterilized packaging

Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes — Amendment 1: Application of risk management

Reference:

ISO 11607-2:2019/Amd 1:2023

Publication Year:

2023

Domain:

Emballage stérile

9 000 F CFA

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Emballages des dispositifs médicaux stérilisés au stade terminal — Partie 2: Exigences de validation pour les procédés de formage, scellage et assemblage — Amendement 1: Application de la gestion des risques

Reference:

ISO 11607-2:2019/Amd 1:2023

Publication Year:

2023

Domain:

Emballage stérile

9 000 F CFA

Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems — Amendment 1: Application of risk management

Reference:

ISO 11607-1:2019/Amd 1:2023

Publication Year:

2023

Domain:

Emballage stérile

9 000 F CFA

Emballages des dispositifs médicaux stérilisés au stade terminal — Partie 1: Exigences relatives aux matériaux, aux systèmes de barrière stérile et aux systèmes d'emballage — Amendement 1: Application de la gestion des risques

Reference:

ISO 11607-1:2019/Amd 1:2023

Publication Year:

2023

Domain:

Emballage stérile

9 000 F CFA

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Sterilized packaging

Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes — Amendment 1: Application of risk management

Emballages des dispositifs médicaux stérilisés au stade terminal — Partie 2: Exigences de validation pour les procédés de formage, scellage et assemblage — Amendement 1: Application de la gestion des risques

Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems — Amendment 1: Application of risk management

Emballages des dispositifs médicaux stérilisés au stade terminal — Partie 1: Exigences relatives aux matériaux, aux systèmes de barrière stérile et aux systèmes d'emballage — Amendement 1: Application de la gestion des risques

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Sterilized packaging

Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes — Amendment 1: Application of risk management

Emballages des dispositifs médicaux stérilisés au stade terminal — Partie 2: Exigences de validation pour les procédés de formage, scellage et assemblage — Amendement 1: Application de la gestion des risques

Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems — Amendment 1: Application of risk management

Emballages des dispositifs médicaux stérilisés au stade terminal — Partie 1: Exigences relatives aux matériaux, aux systèmes de barrière stérile et aux systèmes d'emballage — Amendement 1: Application de la gestion des risques

Pages

LATEST NEWS

Dispelling the fear and embracing the potential of artificial...

PARTNERS

ASN

STANDARDISATION

CERTIFICATION

PROMOTION OF QUALITY