BEUDAMED
    7 results · 36ms · 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 FDA Adverse Event ×

    SURETRACE

    FDA Adverse Event
    Injury ·CONMED UTICA·Product code DRX·April 14, 2026

    SURETRACE

    FDA Adverse Event
    Injury ·CONMED UTICA·Product code DRX·April 14, 2026

    SURETRACE

    FDA Adverse Event
    Injury ·CONMED UTICA·Product code DRX·April 14, 2026

    ENDOTAK C

    FDA Adverse Event
    Injury ·HISTORICAL CPI ST. PAUL·Product code LWS·May 8, 2014

    ASR UNI FEMORAL IMPL SIZE 55

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·October 22, 2012

    EON 16-CHANNEL IPG

    FDA Adverse Event
    Malfunction ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·August 12, 2010

    SMR HUMERAL EXTENSION + 9 MM

    FDA Adverse Event
    Injury ·LIMACORPORATE SPA·Product code KWS·September 28, 2018