FDA-GUDID-FAQS › Unique Device Identifier System: Frequently Asked Questions, Vol. 1 - Guidance for Industry and Food and Drug Administration Staff
FDA-GUDID-FAQS
-
2014 EDITION
-
CURRENT
Unique Device Identifier System: Frequently Asked Questions, Vol. 1 - 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-10993-1Biological evaluation of medical devices
BS-EN-ISO-13485
Medical devices. Quality management systems. Requirements for regulatory purposes
IEC-60601-1
Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
Document Number
FDA-GUDID-FAQS
Revision Level
2014 EDITION
Status
Current
Publication Date
Aug. 20, 2014
Page Count
14 pages