BEUDAMED
    5 results · 24ms · 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 ×

    ACS RX LIFESTREAM CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·ACS/DVI·Product code LOX·March 14, 1997

    FRESENIUS 2008K

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·April 25, 2014

    HARMONIC ACE 23 CM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·November 12, 2007

    PROVENT PROFESSIONAL SLEEP APNEA THERAPY

    FDA Adverse Event
    Injury ·VENTUS MEDICAL·Product code OHP·October 24, 2012

    DELTAPLUSH - PLATINUM MICROCOIL

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code HCG·December 1, 2015