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FOI – 2022-000077 Marketing And Communications team
Information request and response for FOI Reference: FOI – 2022-000077
MHRA Medical Device Safety Information – MDSI2309
MDSI2309 - BioIntegral Surgical Inc. No-React® cardiovascular bioprosthesis implantables: discontinuation of CE marking and manufacture
National programme delivery
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Device Safety Information – DSI/2025/001
DSI/2025/001- Suzhou Surgicare disposable Hysteroscopy Sheath – recall due to withdrawn CE certificate
MHRA Device Safety Information – MDSI2306
MDSI2306 - NuVasive Specialized Orthopedics (NSO) PRECICE Titanium Systems: UK Suspension Lifted
Apply for tender opportunities
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Safety Information Message – SIM2501(U)
SIM2501(U) - Product Safety Report: MK Electric MK Essentials Electrical Three Pin Sockets with Switches: risk of burns
MHRA Medical Device Safety Information – MDSI2311U
MDSI2311U - Specific brands of carbomer eye gel: recall of AACARB eye gel, AACOMER eye gel and PUROPTICS eye gel: potential risk of infection - UPDATE
GP10N(SS) Nurse Prescription Guidance
We are reporting a higher-than-normal presentation of GP10N(SS) Nurse prescriptions forms without a nurse prescriber code printed on them.
Web and channel services
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