Implementation of medical devices future regime
Page summary:
A roadmap outlining the intended timelines for delivering a future regulatory framework for medical devices and an intended policy on international recognition.
Change made:
Updated to include a link to the MHRA’s Consultation on Medical Devices Regulations: Routes to market and in vitro diagnostic devices, and to update the list of topics to be included in the ‘pre-market’ regulations.
Time updated:
12:01am, 14 November 2024
Search the register of customs agents and express operators
Page summary:
Find a customs agent or express operator to help you with import and export declarations.
Change made:
The list of customs agents has been updated with 11 additions.The list of express operators has been updated with 1 addition and one amendment.
Time updated:
8:59am, 14 November 2024
Medical devices: UK approved bodies
Page summary:
UK approved bodies listed under Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002).
Change made:
From the document titled, ‘UL International (UK) medical devices scope’, there was the removal of 4 codes from the UK Approved Body’s designation scope, including MD 0105 – Non-active ophthalmologic devices, MD 1105 – Active ophthalmologic devices, MD 1110 – Active devices for in vitro fertilisation (IVF) and assisted reproductive therapy (ART) and MD 1112 – Medical gas supply systems and parts thereof.
Time updated:
11:15am, 14 November 2024
