BEUDAMED
    8 results · 21ms · 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 ×

    UNK

    FDA Adverse Event
    Injury ·APPLIED MEDICAL RESOURCES·Product code GEI·April 4, 2022

    UNK

    FDA Adverse Event
    Injury ·APPLIED MEDICAL RESOURCES·Product code GEI·April 4, 2022

    SM104 M-SERIES W/5TH WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·March 12, 2013

    QUATTRODE LEAD, 3/6MM, 90 CM

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·February 17, 2011

    AGILIS NXT, 8.5F. STEERABLE INTRODUCER, SMALL CURL

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL·Product code DYB·February 21, 2008

    CARDIOSAVE

    FDA Adverse Event
    Injury ·DATASCOPE CORP.·Product code DSP·April 17, 2014

    CARDIOSAVE HYBRID, TYPE G PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·April 18, 2024

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·November 2, 2021