Standard

CGA/GAS M-23

Published

Singles purchase not accessible

This standard can not be purchased as a single sales.

Abstract

This publication provides clarification on the regulatory classification of medical device gases.  Purpose  This publication will assist in meeting existing FDA and HC requirements on device gas classifications by providing the industry with clarity on the classification of medical device gases to ensure uniform registration and listing across the industry [3, 1].

Document information

  • Standard from CGA/GAS_AC
  • Published:
  • Version: 0
  • Document type: IS
  • Additional information
  • SECOND EDITION