BEUDAMED
    14 results · 22ms · 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 ×

    UNKNOWN

    FDA Adverse Event
    WILLIAM COOK EUROPE·Product code DTK·October 27, 2015

    ECLIPSE RESECT PROTECTOR,SZ M/46.0MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·May 29, 2024

    ECLIPSE RESECT PROTECTOR,SZ L/50.0MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·May 23, 2024

    ECLIPSE RESECT PROTECTOR,SZ M/46.0MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·May 23, 2024

    ECLIPSE RESECT PROTECTOR,SZ S/40.0MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 3, 2024

    AVL 6MM SUPERIOR DRILL, MODULAR

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWE·May 23, 2024

    3.0MM DRILL BIT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HTW·June 7, 2024

    ECLIPSE RESECT PROTECTOR,SZ S/40.0MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·October 1, 2024

    ECLIPSE RESECT PROTECTOR,SZ S/40.0MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·October 1, 2024

    ECLIPSE RESECT PROTECTOR,SZ S/40.0MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·October 1, 2024

    ECLIPSE RESECT PROTECTOR,SZ S/40.0MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·October 1, 2024

    V.A.C. ATS

    FDA Adverse Event
    Injury ·KCI USA INC.·Product code OMP·June 19, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 2, 2013

    ENDEAVOR RESOLUTE RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·December 23, 2010