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UNI EN ISO 10993-9 : 2010

Superseded
Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by
superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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 9: FRAMEWORK FOR IDENTIFICATION AND QUANTIFICATION OF POTENTIAL DEGRADATION PRODUCTS
Superseded date

08-26-2022

Published date

01-01-2010

PREMESSA
INTRODUZIONE
1 SCOPO E CAMPO DI APPLICAZIONE
2 RIFERIMENTI NORMATIVI
3 TERMINI E DEFINIZIONI
4 PRINCIPI PER LA PROGETTAZIONE DEGLI STUDI DI DEGRADAZIONE
5 RESOCONTO DELLO STUDIO
APPENDICE A (normativa) - CONSIDERAZIONI IN MERITO ALLA
  NECESSITA DI CONDURRE DEGLI STUDI DI DEGRADAZIONE
APPENDICE B (informativa) - CONSIDERAZIONI IN MERITO ALLO
  STUDIO DI BIODEGRADAZIONE
APPENDICE ZA (informativa) - RAPPORTO TRA LA PRESENTE NORMA
  EUROPEA E I REQUISITI ESSENZIALI DELLA DIRETTIVA UE
  93/42/CEE CONCERNENTE I DISPOSITIVI MEDICI
APPENDICE ZB (informativa) - RAPPORTO TRA LA PRESENTE NORMA
  INTERNAZIONALE E I REQUISITI ESSENZIALI DELLA DIRETTIVA UE
  90/385/CEE RELATIVA AI DISPOSITIVI MEDICI IMPIANTABILI ATTIVI
BIBLIOGRAFIA

Gives general principles for the systematic evaluation of the potential and observed biodegradation of medical devices and for the design and performance of biodegradation studies.

DocumentType
Standard
PublisherName
Ente Nazionale Italiano di Unificazione (UNI)
Status
Superseded
SupersededBy
Supersedes

ISO/IEC 17025:2005 General requirements for the competence of testing and calibration laboratories
ISO 10993-13:2010 Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices
ISO 10271:2011 Dentistry Corrosion test methods for metallic materials
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 13781:2017 Implants for surgery — Homopolymers, copolymers and blends on poly(lactide) — In vitro degradation testing
ISO 10993-1:2009 Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process

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