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FOI – 2022-000077 Marketing And Communications team
Information request and response for FOI Reference: FOI – 2022-000077
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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DSI/2025/001- Suzhou Surgicare disposable Hysteroscopy Sheath – recall due to withdrawn CE certificate
FOI – 000029 Employee programmes current supplier annual spend and contract renewal date
Information request and response under the Freedom of Information (Scotland) Act 2002
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MHRA Device Safety Information – MDSI2306
MDSI2306 - NuVasive Specialized Orthopedics (NSO) PRECICE Titanium Systems: UK Suspension Lifted