Std

DIN EN ISO 10993-18

Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020 + Amd 1:2022) (includes Amendment A1:2023)

standard by DIN-adopted European-adopted ISO Standard , 11/01/2023

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Product Details

Published:
11/01/2023
Number of Pages:
85
File Size:
1 file , 5.1 MB
Product Code(s):
3477193, 3495512, 3477193, 3495512, 3477193, 3495512
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This product is unavailable in Ukraine, Russia, Belarus
 

Document History

  1. DIN EN ISO 10993-18

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    Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020 + Amd 1:2022) (includes Amendment A1:2023)

    • Most Recent

  2. DIN EN ISO 10993-18/A1 - DRAFT


    Draft Document - Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/DAM 1:2021); German and English version EN ISO 10993-18:2020/prA1:2021

    • Historical Version

  3. DIN EN ISO 10993-18


    Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020); German version EN ISO 10993-18:2020

    • Historical Version

  4. DIN EN ISO 10993-18 - DRAFT


    Draft Document - Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO/DIS 10993-18:2018); German and English version prEN ISO 10993-18:2018

    • Historical Version

  5. DIN EN ISO 10993-18


    Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)

    • Historical Version

  6. DIN EN ISO 10993-18


    Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)

    • Historical Version