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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
Access the Statutory Compliance Audit and Risk Tool (SCART)
Access SCART to report on your health board's legal compliance.
Access the Healthcare Associated Infection System for Controlling Risk in the Built Environment (HAI-SCRIBE)
Access our HAI-SCRIBE tool to manage infection control risks in your health board.
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Access our energy and sustainability resources for health boards.
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Device Safety Information – DSI/2025/001
DSI/2025/001- Suzhou Surgicare disposable Hysteroscopy Sheath – recall due to withdrawn CE certificate
National IT system: Scottish Cervical Call Recall System (SCCRS)
SCCRS is the central IT system that supports the Cervical Screening Programme. Staff can use this area to access relevant documentation.
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