BEUDAMED
    26 results · 47ms · Sources: EU EUDAMED, US FDA

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    WARMING CABINET BW7924TG

    FDA Adverse Event
    Injury ·BLICKMAN INDUSTRIES LLC·Product code LHC·September 8, 2021

    WARMING CABINET BW7924TG

    FDA Adverse Event
    Injury ·BLICKMAN INDUSTRIES LLC·Product code LHC·September 8, 2021

    SALTER LABS

    FDA Adverse Event
    Malfunction ·SALTER LABS·Product code CCW·October 16, 2024

    SALTER LABS

    FDA Adverse Event
    Malfunction ·SALTER LABS·Product code CCW·October 16, 2024

    WHITMEYER HEADREST

    FDA Adverse Event
    Injury ·SUNRISE MEDICAL (US) LLC.·Product code IMS·April 22, 2014

    SALTER LABS

    FDA Adverse Event
    Malfunction ·SALTER LABS·Product code CCW·October 16, 2024

    AIRLIFE

    FDA Adverse Event
    Malfunction ·AIRLIFE·Product code BTT·June 18, 2025

    CMC EXTREMITY PACK

    FDA Adverse Event
    Malfunction ·DEROYAL INDUSTRIES, INC.·Product code LRO·March 3, 2022

    QUICKIE S646

    FDA Adverse Event
    Injury ·SUNRISE MEDICAL (US) LLC.·Product code ITI·August 21, 2012

    TWIIST AUTOMATED INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·MILLYARD ADVANCED MEDICAL PRODUCTS, LLC·Product code QFG·November 12, 2025

    SPNG,GAUZE,4 IN X 4 IN,16 PLY,

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code GDY·May 15, 2024

    LOADING CART FOR 8668 WASHER DISINFECTOR

    FDA Adverse Event
    Malfunction ·GETINGE DISINFECTION AB·Product code MEC·June 25, 2019

    NEXUS® BONESCALPEL® 20MM, UNI-LATERAL SERRATED BLADE + IRRIGATION TUBING KIT

    FDA Adverse Event
    Malfunction ·MISONIX, INC.·Product code LFL·November 6, 2024

    ERBE'S CO2 TUBING/CAP SETS

    FDA Adverse Event
    Injury ·ERBE MEDICAL. LLC·Product code FEQ·April 2, 2026

    ON-Q PAIN PUMP

    FDA Adverse Event
    Injury ·I-FLOW, LLC·Product code MEB·January 8, 2013

    BD SMARTSITE¿ VENTED VIAL ACCESS DEVICE, 13 MM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code LHI·July 29, 2022

    SMARTSITE 20MM VENTED VIAL ACCESS DEVICE

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code LHI·October 1, 2021

    SMARTSITE 20MM VENTED VIAL ACCESS DEVICE

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code LHI·October 1, 2021

    HANAULUX 3000

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·March 28, 2019

    AESCULAP MINOP InVent 30 Trocar System, non-sterile Product Usage:The Minop InVent Trocar System intended use is for endoscopic procedures within the central nervous system, especially for the treatment of intra- and paraventricular pathological structures.

    FDA Recall
    Terminated ·Aesculap Implant Systems LLC·Product code GWG·March 7, 2017