ONORM EN ISO 10993-10 : 2014
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 10: TESTS FOR IRRITATION AND SKIN SENSITIZATION (ISO 10993-10:2010)
07-28-2023
01-12-2013
Dieser Teil der Norm beschreibt Verfahren für die Beurteilung von Medizinprodukten und ihrer Bestandteile hinsichtlich des Hervorrufens einer Irritation und einer Allergie vom verzögerten Typ. Es sind enthalten: a) vor der Prüfung durchzuführende Überlegungen; b) die Durchführung der Prüfung; c) Schlüsselfaktoren bei der Auslegung der Ergebnisse.
| Committee |
TC 179
|
| DocumentType |
Standard
|
| PublisherName |
Osterreichisches Normungsinstitut/Austrian Standards
|
| Status |
Superseded
|
| SupersededBy |
| Standards | Relationship |
| DIN EN ISO 10993-10:2003-02 | Identical |
| NF EN ISO 10993-10 : 2013 | Identical |
| UNE-EN ISO 10993-10:2013 | Identical |
| SN EN ISO 10993-10:2013 | Identical |
| ISO 10993-10:2010 | Identical |
| DIN EN ISO 10993-10:2014-10 | Identical |
| NBN EN ISO 10993-10 : 2013 | Identical |
| I.S. EN ISO 10993-10:2013 | Identical |
| UNI EN ISO 10993-10 : 2013 | Identical |
| NEN EN ISO 10993-10 : 2013 | Identical |
| NS EN ISO 10993-10 : 2013 | Identical |
| BS EN ISO 10993-10:2013 | Identical |
| EN ISO 10993-10:2013 | Identical |
| ONORM EN 14683 : 2014 | MEDICAL FACE MASKS - REQUIREMENTS AND TEST METHODS |
| OVE/ONORM EN 60601-1 : 2014 | MEDICAL ELECTRICAL EQUIPMENT - PART 1: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE (IEC 60601-1:2005 + COR.:2006 + COR.:2007 + A1:2012) |
| ONORM EN 455-3 : 2015 | MEDICAL GLOVES FOR SINGLE USE - PART 3: REQUIREMENTS AND TESTING FOR BIOLOGICAL EVALUATION |
| ISO 10993-13:2010 | Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices |
| ISO 10993-2:2006 | Biological evaluation of medical devices — Part 2: Animal welfare requirements |
| ISO 10993-14:2001 | Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramics |
| ISO 10993-18:2005 | Biological evaluation of medical devices Part 18: Chemical characterization of materials |
| ISO 10993-12:2012 | Biological evaluation of medical devices Part 12: Sample preparation and reference materials |
| ISO 10993-9:2009 | Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products |
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