BEUDAMED
    186 results · 19ms · 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: Injury ×

    IMPLANTABLE NEUROSTIMULATOR

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

    ORSENSE

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

    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

    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

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 14, 2026

    PUMP 381 PUMP SET (US)

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·January 27, 2026

    RP FLEX W SMART ASSIST SET, US

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code PYX·January 20, 2026

    IMPELLA 5.5 WITH SMARTASSIST S2 SET, US

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

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC.·Product code OZD·January 28, 2026

    C-QU MESH

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORPORATION·Product code FTL·January 28, 2021

    TRACER METRO WIRE GU

    FDA Adverse Event
    Injury ·WILSON-COOK MEDICAL, INC.·Product code DQX·March 23, 2004

    FATHOM STRAIGHT TIP STEERABLE GU

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DQX·June 2, 2023