BEUDAMED
    6 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 ×

    8F TRIOX SVO2/CCO PA CATHETERS

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code DQE·April 20, 2016

    8F TRIOX SVO2/CCO PA CATHETERS

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code DQE·April 20, 2016

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·May 17, 2011

    VANGRD ANT STBLZD BRG 10X71

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBH·November 14, 2014

    X8000 LIGHTSOURCE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY·Product code GCT·August 9, 2011

    TOTAL ASR ACET IMP SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 29, 2013