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267 results found
MHRA Device Safety Information – MDSI2305
MDSI2305 - Belzer UW Cold Storage Solution & MPS UW Machine Perfusion Solution manufactured by Carnamedica: Contamination (update to DSI/2023/002)
MHRA Device Safety Information – MDSI (SC) 2106
MDSI (SC) 2106 - Investigation update: CE mark suspended for all MAGEC systems manufactured by NuVasive Specialized Orthopedics, Inc.
MHRA Device Safety Information – MDSI2201
MDSI2201 - Gemini Surgical UK: Stop using all lots and batches of vaginal speculums with smoke tube and gynaecological hysteroscopy sheaths
Testing
Find out more about the tests you can request from the National Microbiology Reference Unit (NMRU).
Safety Alerts
Safety Alerts
Regulation of medical devices and in-vitro diagnostic medical devices
What’s changed with exemptions from medical device regulations.
Guidance - ISO Transition v02
Guidance - ISO Transition v02
Safety Information Message – SIM2209
SIM2209 - UKHSA investigation into potential contamination of bioprosthetic heart valves with Mycobacterium chelonae
MHRA Medical Device Safety Information – MDSI2405
MDSI2405 - Symbios ORIGIN® Posterior Stabilised Patient-Matched Total Knee Replacement Device: Risk of Early Revision
Safety Information Message - SIM2209(U1)
SIM2209(U1) - UKHSA investigation into potential contamination of bioprosthetic heart valves with Mycobacterium chelonae – update (1)