BEUDAMED
    3 results · 18ms · 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 ×

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 2, 2014

    SUPREME EP CATHETER, BIPOLAR, 6F

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC. (AF-MINNETONKA)·Product code DRF·January 24, 2013

    PUMP,COLLEAGUE SINGLE CHANNELCOLOUR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 18, 2010