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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

DSI/2025/001- Suzhou Surgicare disposable Hysteroscopy Sheath – recall due to withdrawn CE certificate

MDSI2309 - BioIntegral Surgical Inc. No-React® cardiovascular bioprosthesis implantables: discontinuation of CE marking and manufacture

MDSI2403 - Counterfeits and unbranded copies of LifeVac anti-choking devices may fail to work correctly or worsen choking incidents if used.

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

Find out how the National Microbiology Reference Unit (NMRU) can support your R&D work.

Information on services offered by our Facilities team.

MDSI (SC) 2106 - Investigation update: CE mark suspended for all MAGEC systems manufactured by NuVasive Specialized Orthopedics, Inc.

Offering essential information to support Scotland’s PMR system suppliers.

This SHTM offers guidance on the technical design and output specifications of partitions.