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DIN EN 12006-3:1999-01

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

NON ACTIVE SURGICAL IMPLANTS - PARTICULAR REQUIREMENTS FOR CARDIAC AND VASCULAR IMPLANTS - PART 3: ENDOVASCULAR DEVICES

Available format(s)

Hardcopy , PDF

Superseded date

01-03-2012

Language(s)

English

Published date

01-01-1999

Foreword
Introduction
1 Scope
2 Normative references
3 Definitions
4 Intended performance
5 Design attributes
6 Materials
7 Design evaluation
8 Manufacturing
9 Sterilization
10 Packaging
11 Information supplied by the manufacturer
Annex A (informative) Bibliography
Annex B (informative) Animal studies with stents
Annex ZA (informative) Relationship between this
         European Standard and the Essential
         Requirements of EU Directive 93/42/EEC

Defines particular requirements for endovascular devices.

DocumentType
Standard
Pages
14
PublisherName
German Institute for Standardisation (Deutsches Institut für Normung)
Status
Superseded

ISO 14630:2012 Non-active surgical implants General requirements
EN ISO 14630:2012 Non-active surgical implants - General requirements (ISO 14630:2012)
ISO 10555-4:2013 Intravascular catheters — Sterile and single-use catheters — Part 4: Balloon dilatation catheters

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