BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    ACCUFLO MONITORING SYSTEM (1800)/ ACCUFLO PROBE (8000)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NA

    FDA UDI
    DEPUY INTERNATIONAL LTD·10603295246534·THOMPSON RASP

    VIVIX-S 1417N

    FDA 510(k)
    FDA Class 2 ·Radiology

    CITRIC ACID 20% SOLUTION, MODEL 329

    FDA 510(k)
    FDA Unclassified ·Unknown

    FIREBIRD SPINAL FIXATION SYSTEM, PHEONIX MIS

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code NKB·June 18, 2014

    RENEW SINGLE RECEIVER

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION DIVISION·Product code GZB·December 21, 2010

    C-QUR VPATCH

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORP.·Product code FTL·January 2, 2013