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Norm
ÖVE/ÖNORM EN ISO 13488
Issue date: 2001 04 01
Quality systems - Medical devices - Particular requirements for the application of EN ISO 9002 (revision of EN 46002:1996) (identical to ISO 13488:1996)
Withdrawn: 2003 11 01
§ Legal References
Publisher:
Austrian Standards International
Format:
Digital | 13 Pages
Language:
German
Currently valid:
Optionally co-design standards:
ÖVE/ÖNORM EN ISO 13485
2022 02 01
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)...
Norm
ÖVE/ÖNORM EN ISO 13485
2017 08 01
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)...
Norm
ÖVE/ÖNORM EN ISO 13485
2016 07 01
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)...
Norm
ÖNORM EN ISO 13485
2012 11 01
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003 ...
Norm
ÖNORM EN ISO 13485
2010 02 15
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003 ...
Norm
ÖNORM EN ISO 13485
2007 11 01
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003)...
Norm
ÖNORM EN ISO 13485
2003 11 01
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003)...
Norm
ÖVE/ÖNORM EN ISO 13488
2001 04 01
Quality systems - Medical devices - Particular requirements for the application of EN ISO 9002 (revi...
Norm
↖
ÖNORM EN 46002
1996 12 01
Quality systems - Medical devices - Particular requirements for the application of EN ISO 9002
Norm
ÖNORM EN 46002
1994 02 01
Quality systems - Medical devices - Particular requirements for the application of EN 29002
Norm
Norm
Issue date :
1996 12 26
Quality systems — Medical devices — Particular requirements for the application of ISO 9002
Norm
Issue date :
1994 06 30
Quality systems — Model for quality assurance in production, installation and servicing
Norm
Issue date :
1995 03 09
Sterilization of health care products — Requirements for validation and routine control — Radiation sterilization
Norm
Issue date :
2003 11 01
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003)