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

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    GELIPERM DRY

    FDA 510(k)
    FDA Unclassified ·Unknown

    HEARTLINE RECEIVING STATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ELI 280 ELECTROCARDIOGRAPH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NC TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·May 20, 2014

    CURLIN 6000 PAINSMART IOD IV PUMP

    FDA Adverse Event
    Malfunction ·MOOG MEDICAL DEVICES GROUP·Product code FRN·October 9, 2012

    BRAVO

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD.·Product code FFT·August 22, 2010

    UNKNOWN SHOULDER COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·April 16, 2024