BEUDAMED
    11 results · 31ms · 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 ×

    BD SEDI-40

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·July 13, 2021

    MICROSTAAR® INJECTOR

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL COMPANY·Product code KYB·February 26, 2016

    TAXUS¿ LIBERTÉ¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·March 12, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·February 18, 2011

    RESUME

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code GZF·February 19, 2008

    SYSTEM 5000 ESU- ENGLISH- 120V

    FDA Adverse Event
    Malfunction ·CONMED ELECTROSURGERY·Product code GEI·September 22, 2017

    STERILE 3.0 SOFT KOH-EFF

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HEW·February 20, 2019

    CARDIOHELP

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·March 17, 2025

    ICAST COVERED STENT SYSTEM, 6MMX22MMX120CM

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code PRL·November 7, 2025

    ICAST COVERED STENT SYSTEM, 7MMX22MMX120CM

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code PRL·November 7, 2025

    AUTO ENDO5 ML

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code FZP·June 7, 2019