Standard

ISO/DIS 10993-11

Draft

Note: Latest version: ISO 10993-11:2017

Existing or new amendments and versions must be purchased separately.

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Abstract

ISO 10993-11:2017 specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.

Products specifications

  • Standard from ISO
  • Period for objection until:
  • Edition: 4
  • Document type: IS
  • Pages
  • Publisher: ISO
  • Distributor: ISO
  • ICS: 11.100.20
  • International TC: ISO/TC 194

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