Unique Device Identification: Direct Marking of Devices : Guidance for Industry and Food and Drug Administration Staff
Information
Type
Guidance
Regulated products
Biologics, Medical Devices
Topics
Labeling, UDI
Published
November 17, 2017
Last updated
July 15, 2021
Description
This document is a guidance for labeling and direct marking of devices, specifically focusing on Unique Device Identification (UDI).
Tags
Organization
Country / Region
United States
License
Other (Public Domain)