BEUDAMED
    5 results · 29ms · 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 ×

    HU-FRIEDY PERMA SHARP SUTURES

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code GAR·May 26, 2010

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·March 20, 2019

    FENESTRATED BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·January 25, 2013

    Z-5 ATRIOSEPTOSTOMY CATHETER

    FDA Adverse Event
    Malfunction ·NUMED CANADA, INC.·Product code DQO·November 18, 2010

    CAPSUREEPI

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·July 11, 2014