BEUDAMED
    5 results · 16ms · 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 Status: Malfunction ×

    OXFORD UNI KNEE PHASE III 4.0MM DIAM. FEMORAL DRILL

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code HTW·November 20, 2009

    OXFORD MP 04MM DRILL

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code NRA·April 13, 2017

    OXFORD PH3 CEMENTLESS FEM SZ M

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code NRA·June 20, 2025

    AXSYM DIGOXIN III

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

    TRUSTEEL

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·May 22, 2025