MHRA
Medicines and Healthcare products Regulatory Agency
About
MHRA regulates medical devices in the United Kingdom following Brexit. It oversees device registration, UKCA marking, market surveillance, yellow card vigilance reporting, and clinical investigations.
Regulatory Details
Regulatory FrameworkUK MDR 2002 (as amended post-Brexit)
Device ClassificationClass I, Class IIa, Class IIb, Class III
Jurisdiction TypeNational
Country🇬🇧 United Kingdom
StatusActive