CEI UNI EN/ISO 13485
Medical devices - Quality management systems - Requirements for regulatory purposes
active, Most Current
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| Organization: | CEI |
| Publication Date: | 1 November 2017 |
| Status: | active |
| Page Count: | 22 |
| ICS Code (Quality management and quality assurance): | 03.120.10 |
| ICS Code (Medical equipment in general): | 11.040.01 |
Document History
CEI UNI EN/ISO 13485
November 1, 2017
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
April 1, 2016
Medical devices - Quality management systems - Requirements for regulatory purposes
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...
April 1, 2012
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...