SN EN 46002 : 1997
Current
The latest, up-to-date edition.
QUALITY SYSTEMS - MEDICAL DEVICES - PARTICULAR REQUIREMENTS FOR THE APPLICATION OF EN ISO 9002
12-01-2013
Cooperating organizations
National foreword
Foreword
0. Introduction
1. Scope and field of application
2. Normative references
3. Definitions
4. Quality system requirements
4.1 Management responsibility
4.2 Quality system
4.3 Contract review
4.4 Document control
4.5 Purchasing
4.6 Purchaser supplied product
4.7 Product identification and traceability
4.8 Process control
4.9 Inspection and testing
4.10 Inspection, measuring and test equipment
4.11 Inspection and test status
4.12 Control of nonconforming product
4.13 Corrective action
4.14 Handling, storage, packaging and delivery
4.15 Quality records
4.16 Internal quality audits
4.17 Training
4.18 Statistical techniques
Annex A (informative) - Bibliography
National annex NA (informative) Committees responsible
National annex NB (informative) Cross-references
Specifies the quality requirements for the production and, where relevant, installation of medical devices. Coverage includes: quality system requirements; product identification and traceability; inspection, measuring and test equipment; control of nonconforming product; handling, storage, packaging and delivery; internal quality audits. Also gives detailed definitions.
DevelopmentNote |
To be read in conjunction with EN ISO 9002. (08/2002)
|
DocumentType |
Standard
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PublisherName |
Swiss Standards
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Status |
Current
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Standards | Relationship |
BS EN 46002:1997 | Identical |
I.S. EN 46002:1997 | Identical |
DIN EN 46002:1996-09 | Identical |
EN 46002 : 1996 | Identical |
UNE-EN 46002:1996 | Identical |
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