2017/746 REGULATION (EU) 2017/746 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU

2017/746 - 2017 EDITION - CURRENT -- See the following: 2022/112


Included in this current edition are the following subparts:

 2017 EDITION - April 5, 2017
 2017 EDITION CORRIGENDUM 1 - May 3, 2019
 2017 EDITION CORRIGENDUM 2 - Dec. 27, 2019
 FOR AMENDMENT 1 SEE 2022/112 - Jan. 25, 2022


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-13485
Medical devices. Quality management systems. Requirements for regulatory purposes

BS-EN-ISO-14971
Medical devices. Application of risk management to medical devices

BS-EN-ISO-15223-1
Medical devices. Symbols to be used with information to be supplied by the manufacturer

ORDER

Price:

$36.00        




Document Number

REGULATION (EU) 2017/746

Revision Level

2017 EDITION

Status

Current

Publication Date

April 5, 2017

Page Count

157 pages