BEUDAMED
    11 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    IMPELLA RP PUMP

    FDA Adverse Event
    Malfunction ·ABIOMED, INC.·Product code OZD·February 6, 2020

    IMPELLA 5.0

    FDA Adverse Event
    Death ·ABIOMED INC.·Product code OZD·February 3, 2022

    ADVANTA V12,COVERED STENT SYS,9X59X80

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·April 7, 2026

    EXABLATE MRGFUS

    FDA Adverse Event
    Injury ·INSIGHTEC, LTD.·Product code NRZ·August 29, 2017

    PFC*SIGMA C/S NPOR FEM RT SZ 5

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·May 31, 2013

    9617604-2008-00079

    FDA Adverse Event
    Malfunction ·Product code BTR·June 12, 2008

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·June 25, 2011

    ADVANTA V12 COVERED STENT SYSTEM

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORPORATION·Product code NIO·August 13, 2025

    ADVANTA V12 COVERED STENT

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·September 10, 2025

    ADVANTA V12,COVERED STENTSYS, 9X59X120

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·January 12, 2026

    ADVANTAV12,COVERED STENTSYS, 6X59X120

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·January 12, 2026