BEUDAMED
    7 results · 26ms · 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.

    GRAHAM-FIELD ELECTRODE CONDUCTIVITY GEL

    FDA 510(k)
    FDA Class 2 ·Neurology

    LARIAT CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACCU PATH STERILE LABEL

    FDA 510(k)

    BERLIN HEART EXCOR PEDIATRIC VAD

    FDA Adverse Event
    Injury ·BERLIN HEART GMBH·Product code DSQ·June 19, 2014

    GRASPING RETRACTOR INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·February 5, 2013

    THINLINE

    FDA Adverse Event
    Injury ·GUIDANT ANGLETON/ST. PAUL·Product code NVN·January 3, 2011

    EVOLUT FX PLUS VALVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code NPT·September 17, 2025