BS EN 12006-3 : 1999
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
NON-ACTIVE SURGICAL IMPLANTS - PARTICULAR REQUIREMENTS FOR CARDIAC AND VASCULAR IMPLANTS - PART 3: ENDOVASCULAR DEVICES
Hardcopy , PDF
30-06-2011
English
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
Describes the particular requirements for endovascular devices.
Committee |
CH/150/2
|
DevelopmentNote |
Supersedes 96/563256 DC. (08/2005) 1998 Edition Re-Issued in December 2009 & incorporates AMD 1 2009. (12/2009)
|
DocumentType |
Standard
|
Pages |
10
|
PublisherName |
British Standards Institution
|
Status |
Superseded
|
SupersededBy | |
Supersedes |
Standards | Relationship |
UNI EN 12006-3 : 2009 | Identical |
UNE-EN 12006-3:1999 | Identical |
DIN EN 12006-3:2009-08 | Identical |
NBN EN 12006-3 : 1999 + A1 2009 | Identical |
NS EN 12006-3 : 1998 + A1 2009 | Identical |
EN 12006-3:1998+A1:2009 | Identical |
NF EN 12006-3 : 1999 + A1 2009 | Identical |
NEN EN 12006-3 : 1998 + A1 2009 | Identical |
I.S. EN 12006-3:1999 | Identical |
SN EN 12006-3 : 1999 + A1 2009 | Identical |
DIN EN 12006-3:1999-01 | Identical |
NFS 91 141 : 1997 | BIODEGRADABILITY OF DENTAL METAL ALLOYS - STANDARDIZATION OF ELECTROCHEMICAL TESTS |
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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