FDA-UDI-FORM Unique Device Identification System: Form and Content of the Unique Device Identifier (UDI) - Draft Guidance for Industry and Food and Drug Administration Staff

FDA-UDI-FORM - 2021 EDITION - CURRENT
Show Complete Document History


Unique Device Identification System: Form and Content of the Unique Device Identifier (UDI) - Draft Guidance for Industry and Food and Drug Administration Staff


This document comes with our free Notification Service, good for the life of the document.

This document is available in either Paper or PDF format.

 

Customers who bought this document also bought:

BS-EN-ISO-20417
Medical devices. Information to be supplied by the manufacturer

2017/745
REGULATION (EU) 2017/745 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC

MHLW-169
Ministry of Health, Labor & Welfare Ordinance No. 169 (QMS)

ORDER

Price:

$20.00        




Document Number

GUD1500035-2021

Revision Level

2021 EDITION

Status

Current

Publication Date

July 7, 2021

Page Count

10 pages