FDA-CYBERSECURITY-MA › Postmarket Management of Cybersecurity in Medical Devices
Postmarket Management of Cybersecurity in Medical Devices
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:
2017/745REGULATION (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
IEC-60529
Degrees of protection provided by enclosures (IP Code)
IEC-60601-1
Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
Document Number
FDA-CYBERSECURITY-MA
Revision Level
2016 EDITION
Status
Current
Publication Date
Dec. 28, 2016
Page Count
30 pages