ISO/TS 19218:2005 specifies requirements for a coding structure for describing adverse events related to medical devices. This code is intended for use by medical device users, manufacturers and regulatory authorities.
Status: WithdrawnPublication date: 2005-11
Edition: 1Number of pages: 11
Technical Committee: ISO/TC 210 Quality management and corresponding general aspects for products with a health purpose including medical devices
ISO/TS 19218:2005Stage: 95.99
Got a question?
Check out our FAQs
+41 22 749 08 88
Monday to Friday - 09:00-12:00, 14:00-17:00 (UTC+1)
Keep up to date with ISO
Sign up to our newsletter for the latest news, views and product information.