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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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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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