CGA M-23

This publication provides clarification on the regulatory classification of medical device gas mixtures.

This publication will assist in meeting existing FDA and Health Canada 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.

Edition:

1st

Published:

09/24/2019

Number of Pages:

10

File Size:

1 file , 980 KB

Note:

This product is unavailable in Russia, Ukraine, Belarus