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BSI - BS EN ISO 13485 + A11

Medical devices - Quality management systems - Requirements for regulatory purposes

active, Most Current
Organization: BSI
Publication Date: 31 March 2016
Status: active
Page Count: 90
ICS Code (Quality management and quality assurance): 03.120.10
ICS Code (Medical equipment in general): 11.040.01
ICS Code (Management systems): 03.100.70

Document History

March 31, 2016
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
BS EN ISO 13485 + A11
March 31, 2016
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
March 31, 2016
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
March 31, 2016
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
February 29, 2016
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
March 31, 2012
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
March 31, 2012
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
July 24, 2003
Medical devices Quality management systems Requirements for regulatory purposes
General  This International Standard specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that...
July 24, 2003
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
July 24, 2003
Medical devices - Quality management systems - Requirements for regulatory purposes
General  This International Standard specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that...
March 15, 2001
Quality Systems - Medical Devices - Particular Requirements for the Application of EN ISO 9001
To be read in conjunction with BS EN ISO 9001:1994

References

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