BEUDAMED
    8 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 ×

    COMFORT

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 23, 2026

    AMS 700 LGX

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code JCW·September 23, 2025

    AMS 700 LGX

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code JCW·September 2, 2025

    NOVASURE

    FDA Adverse Event
    Injury ·HOLOGIC, INC.·Product code MNB·January 8, 2025

    AXSYM DIGOXIN III

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

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013

    REFURBED COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - BUFFALO GROVE·Product code FRN·March 8, 2011

    AMS 700 LGX

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code JCW·January 19, 2026