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EN 46002 : 1996

Superseded

Superseded

View Superseded by

QUALITY SYSTEMS - MEDICAL DEVICES - PARTICULAR REQUIREMENTS FOR THE APPLICATION OF EN ISO 9002

Published date

01-12-2013

Superseded date

10-25-2000

Superseded by

EN ISO 13488 : 2000

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Summarise this standard

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.

Committee
CEN/CLC CWG/QS
DevelopmentNote
Renumbered to EN ISO 13488 (05/2001)
DocumentType
Standard
PublisherName
Comite Europeen de Normalisation
Status
Superseded
SupersededBy

Standards Relationship
NF EN 46002 : 1996 Identical
NBN EN 46002 : 1996 Identical
NEN EN 46002 : 1996 Identical
I.S. EN 46002:1997 Identical
BS EN 46002:1997 Identical
CEI EN 46002 : 2ED 1996 Identical
DIN EN 46002:1996-09 Identical
UNE-EN 46002:1996 Identical

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