BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

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    SURGIDEK B

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814268·GENUMEDI PT SILVER R III

    DEPUY CAS KNEE INSTRUMENTATION

    FDA 510(k)
    FDA Class 2 ·Neurology

    CGBA-032A, Aquilion PRIME Self-Propelled Scan Base Kit for IVR-CT

    FDA 510(k)
    FDA Class 2 ·Radiology

    INTEGRATED APD SET W/CASSETTE3-PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·December 30, 2010

    QUICKSET 1PC FLEX DRILL BIT 30

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·July 18, 2014

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·December 12, 2012

    Philips Zenition 50, Model Number: 718096

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024