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DIN EN ISO 10993-15

Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000); German version EN ISO 10993-15:2009

active, Most Current
Organization: DIN
Publication Date: 1 October 2009
Status: active
Page Count: 21
ICS Code (Biological evaluation of medical devices): 11.100.20

Document History

DIN EN ISO 10993-15
May 1, 2018
Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO/DIS 10993-15:2018); German and English version prEN ISO 10993-15:2018
A description is not available for this item.
DIN EN ISO 10993-15
October 1, 2009
Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000); German version EN ISO 10993-15:2009
A description is not available for this item.
DIN EN ISO 10993-15/A1
March 1, 2009
Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000); English version FprEN ISO 10993-15:2009, Amendment 1
A description is not available for this item.
DIN EN ISO 10993-15
November 1, 2001
Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000); German version EN ISO 10993-15:2000
A description is not available for this item.
DIN EN ISO 10993-15
May 1, 1999
Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO/DIS 10993-15:1998); German version prEN ISO 10993-15:1998
A description is not available for this item.

References

This document is referenced by:
DIN EN ISO 10993-10 - Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010); German version EN ISO 10993-10:2013
Published by DIN on October 1, 2014
Dieser Teil der ISO 10993 beschreibt das Verfahren für die Beurteilung von Medizinprodukten und ihren Bestandteilen hinsichtlich ihres Potentials, eine Irritation und eine Hautsensibilisierung...
This document is referenced by:
DIN EN ISO 10993-10 - Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010)
Published by DIN on October 1, 2014
This part of ISO 10993 describes the procedure for the assessment of medical devices and their constituent materials with regard to their potential to produce irritation and skin sensitization. This...
This document is referenced by:
DIN EN ISO 10993-12 - Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012); German version EN ISO 10993-12:2012
Published by DIN on October 1, 2012
Der vorliegende Teil der ISO 10993 legt Anforderungen fest und gibt Anleitungen zu Verfahren, die bei der Probenvorbereitung und bei der Auswahl von Referenzmaterialien für die biologische Prüfung...
This document is referenced by:
DIN EN ISO 7198 - Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches (ISO 7198:2016); German version EN ISO 7198:2017
Published by DIN on July 1, 2017
Diese Internationale Norm legt, beruhend auf dem gegenwärtigen medizinischen Wissensstand, Anforderungen an die Bewertung von Gefäßprothesen sowie Anforderungen an Nomenklatur, Konstruktionsmerkmale...
This document is referenced by:
DIN EN ISO 10993-4 - Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017); German version EN ISO 10993-4:2017
Published by DIN on December 1, 2017
Dieses Dokument legt allgemeine Anforderungen zur Beurteilung der Wechselwirkungen von Medizinprodukten mit Blut fest. Dieser Teil enthält: a) eine Klassifizierung von für den Kontakt mit Blut...
This document is referenced by:
DIN EN 13060 - Small steam sterilizers; German version EN 13060:2014+A1:2018
Published by DIN on February 1, 2019
Diese Europäische Norm legt die Leistungsanforderungen und Prüfverfahren für Dampf-Klein-Sterilisatoren und deren Sterilisationszyklen fest, die für medizinische Zwecke oder für Materialien verwendet...
This document is referenced by:
DIN EN ISO 7405 - Dentistry - Evaluation of biocompatibility of medical devices used in dentistry (ISO 7405:2018, Corrected version 2018-12); German version EN ISO 7405:2018
Published by DIN on March 1, 2019
Dieses Dokument legt Prüfverfahren zur Beurteilung der biologischen Wirkungen von in der Zahnheilkunde verwendeten Medizinprodukten fest. Enthalten sind auch Prüfungen von pharmakologischen Stoffen,...
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