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Superseded
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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
Superseded date
21-12-2019
Language(s)
German
Published date
01-01-2016
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Superseded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 |
SN EN ISO 10993-16 : 2010 | Identical |
UNI EN ISO 10993-16 : 2010 | Identical |
UNE-EN ISO 10993-16:2010 | Identical |
NF EN ISO 10993-16 : 2017 | Identical |
ONORM EN ISO 10993-16 : 2018 | 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) |
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