CFR 21-830.340-2013
Food and Drugs. Part830:Unique device identification. Section830.340:Voluntary submission of ancillary device identification information.

Standard No.

CFR 21-830.340-2013

Release Date

2013

Published By

US-CFR-file

Latest

CFR 21-830.340-2013

Scope

(a) You may not submit any information to the Global Unique Device Identification Database (GUDID) other than that specified by § 830.310, except where FDA acts to permit the submission of specified additional types of information, termed ancillary inform

CFR 21-830.340-2013 history

• 2013 CFR 21-830.340-2013 Food and Drugs. Part830:Unique device identification. Section830.340:Voluntary submission of ancillary device identification information.