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Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Check the tariff classification of multifunctional display-monitors for vehicles.
From 1 April, Monitor is part of NHS Improvement.
A digital platform designed to facilitate the reporting, monitoring, and management of medical device incidents.
Advice for manufacturers of Class I medical devices for placing products on the UK market
References to normative documents for measuring instruments in support of the Measuring Instruments Regulations 2016.
Guidance on the updates to reporting forms following implementation of the Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024.
Product Safety Report for Aisilan Surface Mounted Spotlight presenting a serious risk of electric shock due to inadequate earthing and the potential for accessible metal parts to become live.
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