DIN EN ISO 10993-16:2016-04 (Draft)
Superseded
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 16: TOXICOKINETIC STUDY DESIGN FOR DEGRADATION PRODUCTS AND LEACHABLES (ISO 10993-16:2017)
Available format(s)
Hardcopy , PDF
Language(s)
German
Published date
01-01-2016
Superseded date
21-12-2019
£80.20
Excluding VAT
| DocumentType |
Draft
|
| Pages |
43
|
| PublisherName |
German Institute for Standardisation (Deutsches Institut für Normung)
|
| Status |
Superseded
|
| Standards | Relationship |
| NBN EN ISO 10993-16 : 2010 | Identical |
| I.S. EN ISO 10993-16:2010 | Identical |
| BS EN ISO 10993-16:2010 | Identical |
| ISO 10993-16:2017 | Identical |
| NF EN ISO 10993-16 : 2017 | Identical |
| UNE-EN ISO 10993-16:2010 | Identical |
| NEN EN ISO 10993-16 : 2018 | Identical |
| BS EN ISO 10993-16:2017 | Identical |
| EN ISO 10993-16:2017 | Identical |
| NS EN ISO 10993-16 : 2017 | Identical |
| I.S. EN ISO 10993-16:2017 | Identical |
| DIN EN ISO 10993-1:2010-04 | Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management system (ISO 10993-1:2009) |
| DIN EN ISO 10993-15:2009-10 | Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000) |
| DIN EN ISO 10993-6:2009-08 | BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION (ISO 10993-6:2016) |
Summarise
£80.20
Excluding VAT
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