The Medical Devices (Amendment etc.) (EU Exit) Regulations 2020
Information
Type
Regulation
Regulated products
Medical Devices
Published
December 8, 2020
Last updated
December 8, 2020
Description
These Regulations are made in exercise of the powers in sections 8(1) and 8C of the European Union (Withdrawal) Act 2018 (c. 16) in order to address failures of retained EU law to operate effectively and other deficiencies (in particular under section 8(2)(a)) arising from the withdrawal of the United Kingdom from the European Union, and in order to give effect to the Protocol on Ireland/Northern Ireland in the withdrawal agreement, respectively.
Tags
Organization
Country / Region
United Kingdom
License
Open Government Licence 3.0 (United Kingdom)