The Medical Devices (Amendment) Regulations 2013
Information
Type
Regulation
Regulated products
Medical Devices
Published
September 12, 2013
Last updated
September 12, 2013
Description
These Regulations amend the Medical Devices Regulation 2002 (the 2002 Regulations) in order to implement Commission Regulation (EU) No 207/2012 of 9 March 2012 on electronic instructions for use of medical devices and Commission Regulation (EU) No 722/2012 of 8 August 2012 concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin.
Tags
Organization
Country / Region
United Kingdom
License
Open Government Licence 3.0 (United Kingdom)