BEUDAMED
    1,179 results · 23ms · 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 ×

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code MHY·July 7, 2023

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·July 7, 2023

    FINGER SENSOR USED BY ONEBLOOD DONATION CENTER

    FDA Adverse Event
    Malfunction ·UNK·Product code QGU·June 28, 2022

    ORSENSE

    FDA Adverse Event
    Injury ·ORSENSE LTD·Product code QGU·June 11, 2025

    NBM-200

    FDA Adverse Event
    Malfunction ·ORSENSE LTD.·Product code QGU·March 14, 2026

    NBM-200

    FDA Adverse Event
    Malfunction ·ORSENSE LTD.·Product code QGU·March 14, 2026

    THUMB HGB MONITOR

    FDA Adverse Event
    Malfunction ·ORSENSE LTD.·Product code QGU·January 7, 2025

    THUMB HGB MONITOR

    FDA Adverse Event
    Malfunction ·ORSENSE LTD.·Product code QGU·January 7, 2025

    U.S.S.C. BIOSYN 2/0 U/D GU-45

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL CORP.·Product code GAN·May 25, 2000

    SPACEOAR SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OVB·January 2, 2026

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·February 19, 2026

    ECP PUMP SET

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·January 29, 2026

    PUMP 371 14F LT CMR SET

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 11, 2026

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·January 22, 2026

    PUMP 381 PUMP SET (US)

    FDA Adverse Event
    Death ·ABIOMED, INC. - 1220648·Product code OZD·January 26, 2026

    RP FLEX W SMART ASSIST SET, US

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code PYX·February 4, 2026

    PUMP 381 PUMP SET (US)

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·January 23, 2026

    PUMP 381 PUMP SET (US)

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·January 29, 2026

    UNKNOWN ENT REFLEX ULTRA PLASMA WAND AND TURBINATOR WAND

    FDA Adverse Event
    Injury ·ARTHROCARE CORPORATION·Product code GEI·November 24, 2022

    IMPELLA 5.5

    FDA Adverse Event
    Injury ·ABIOMED, INC.·Product code OZD·January 19, 2026