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Norm

ÖNORM EN 46002

Issue date: 1994 02 01

Quality systems - Medical devices - Particular requirements for the application of EN 29002

Withdrawn: 1996 12 01
Publisher:
Austrian Standards International
Format:
Paper | 8 Pages
Language:
German
Currently valid:
ÖVE/ÖNORM EN ISO 13485:2022 02 01
Optionally co-design standards:
Committee 129: Quality Management Systems and Business Excellence
Norm timeline
Normative References
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
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
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
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
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
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
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
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
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Norm
ÖNORM EN 46002
Issue date : 1996 12 01
Quality systems - Medical devices - Particular requirements for the application of EN ISO 9002

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