BEUDAMED
    12 results · 39ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GORE TIGRIS® VASCULAR STENT

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·October 11, 2016

    ADVANTA V12,COVERED STENT SYS,9X59X80

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

    OXFORD UNICOMPARTMENTAL KNEE ARCOM MENISCAL BEARING LARGE RIGHT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·July 13, 2011

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·June 10, 2013

    GE OEC 8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 12, 2008

    IMPELLA RP PUMP

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

    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

    GORE TIGRIS® VASCULAR STENT

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·September 6, 2016

    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

    IMPELLA 5.0

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