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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

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Device Safety Information – DSI/2025/001

DSI/2025/001- Suzhou Surgicare disposable Hysteroscopy Sheath – recall due to withdrawn CE certificate

Decontamination of flexible thermolabile endoscopes and TOE ultrasound probes (SHTM 01-06)

Scottish Health Technical Memorandum 01-06 Parts A–E: decontamination of flexible thermolabile endoscopes and TOE ultrasound probes in EDUs

MHRA Device Safety Information – MDSI2306

MDSI2306 - NuVasive Specialized Orthopedics (NSO) PRECICE Titanium Systems: UK Suspension Lifted

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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

The power of inertia

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