The Medical Devices (Amendment) Regulations 2013
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.
Lifecycle
Department
Made
12 Sept 2013
—
In force
21 Oct 2013
Enabling power
The Secretary of State has consulted such organisations that appear to him to be representative of the interests substantially affected by these Regulations, such other persons as he considers appropriate and the Health and Safety Executive in accordance with section 11(5) of the Consumer Protection Act 1987.
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