BEUDAMED
    11 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    HS1 DEFIBRILLATOR, FRENCH, EXCHANGE

    FDA Adverse Event
    Malfunction ·PHILIPS NORTH AMERICA LLC·Product code MKJ·February 21, 2023

    AED PHILIPS ADULT SMART PADS CARTRIDGE

    FDA Adverse Event
    Malfunction ·PHILIPS NORTH AMERICA LLC.·Product code MKJ·July 19, 2022

    GMK-SPHERE TIBIAL INSERT FIXED FLEX SIZE 5/10 MM LEFT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 27, 2016

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 23, 2025

    GMK-SPHERE TIBIAL INSERT FIXED FLEX SIZE 5/10 MM LEFT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·April 21, 2017

    RESOLUTE ONYX RX

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIQ·January 31, 2019

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIQ·April 9, 2019

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2014

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 10, 2013

    LIGAMAX- CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 13, 2011

    RESOLUTE ONYX RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·July 1, 2021