AS ISO 14630-2003
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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Non-active surgical implants - General requirements
Hardcopy , PDF 1 User , PDF 3 Users , PDF 5 Users , PDF 9 Users
30-06-2017
English
01-01-2003
Important note : Users cannot be edited or removed once added to your Multi user PDF.Specifies general requirements for non-active surgical implants. It is not applicable to dental implants, dental restorative materials, transendodontic and transradicular implants and intra-ocular lenses. With regard to safety, ISO 14630 gives requirements for intended performance, design attributes, materials, design evaluation, manufacture, sterilization, packaging and information supplied by the manufacturer, and tests.
| Committee |
HE-012
|
| DocumentType |
Standard
|
| ISBN |
0 7337 5342 6
|
| Pages |
9
|
| PublisherName |
Standards Australia
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes | |
| UnderRevision |
This European Standard specifies general requirements for non-active surgical implants.This standard is not applicable to dental implants, dental restorative materials,transendodontic and transradicular implants and intra-ocular lenses.With regard to safety, this standard gives requirements for intended performance, designattributes, materials, design evaluation, manufacture, sterilization, packaging andinformation supplied by the manufacturer, and tests.Tests required to be used to demonstrate compliance with this standard are contained inother levels.
| Standards | Relationship |
| ISO 14630:1997 | Identical |
First published as AS ISO 14630-2003.
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