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MHRA Device Safety Information – MDSI2303
MDSI2303 - Zimmer Biomet NexGen Knee replacement: affected patients should be offered additional follow up.
MHRA Medical Device Safety Information – MDSI2309
MDSI2309 - BioIntegral Surgical Inc. No-React® cardiovascular bioprosthesis implantables: discontinuation of CE marking and manufacture
A health economic analysis of the introduction of a cell collection system (Cytosponge®) as a viable alternative to upper GI endoscopy in the COVID recovery
A project looking at the viability of a cell collection system alternative for COVID recovery
MHRA Medical Device Safety Information – MDSI2405
MDSI2405 - Symbios ORIGIN® Posterior Stabilised Patient-Matched Total Knee Replacement Device: Risk of Early Revision
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Check the latest medical devices alerts (MDA).
MHRA Device Safety Information (MDSI)
MHRA Device Safety Information (MDSI) MDSIs capture safety information from MHRA. The information is about safety concerns which do not meet MHRAs cri
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