CFR 21-830.300-2013
Food and Drugs. Part830:Unique device identification. Section830.300:Devices subject to device identification data submission requirements.

Standard No.

CFR 21-830.300-2013

Release Date

2013

Published By

US-CFR-file

Latest

CFR 21-830.300-2013

Scope

(a) In general. The labeler of a device must provide the information required by this subpart for each version or model required to bear a unique device identifier (UDI).

CFR 21-830.300-2013 history

• 2013 CFR 21-830.300-2013 Food and Drugs. Part830:Unique device identification. Section830.300:Devices subject to device identification data submission requirements.