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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    AMDINOCILLIN 10 MCG SENSI-DISC

    FDA 510(k)
    FDA Class 2 ·Microbiology

    CAMCERAM TCP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Reprocessed Electrophysiology Diagnostic Catheters

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PROPAQ MD DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 18, 2014

    NC QUANTUM APEX¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·November 29, 2012

    U-BLADE LAG SCREW CONNECTOR

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·September 20, 2010