BEUDAMED
    66 results · 23ms · Sources: EU EUDAMED, US FDA

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    CARDIOSAVE Hybrid Intra-Aortic Balloon Pump

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Oticon

    FDA UDI
    Oticon A/S·05707131288196·NERA2 PRO, DESIGNRITE 10 WL VLI

    NEWFIX SCREW, WIRE AND PIN FIXARION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PERIPHERAL CUTTING BALLOON

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD SAFETYGLIDE¿ INSULIN SYRINGE WITH ATTACHED NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·January 25, 2022

    BD SAFETYGLIDE¿ NEEDLE 1-ML SYRINGE WITH 25-G X 5/8-IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 22, 2022

    BD SAFETYGLIDE¿ NEEDLE 1-ML SYRINGE WITH 25-G X 5/8-IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMI·February 17, 2022

    BD SAFETYGLIDE¿ INSULIN SYRINGE WITH ATTACHED NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·December 14, 2021

    BD LUER-LOK¿ SYRINGE WITH BD SAFETYGLIDE¿ SAFETY NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·January 27, 2020

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 7, 2013

    AUGMENTED INSERT

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 30, 2011

    QC F/K-WIRES Ø0.6-3.2 F/532.001 532.010

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·October 8, 2014

    840 VENTILATOR

    FDA Adverse Event
    Injury ·COVIDIEN·Product code CBK·June 20, 2017

    1 ML BD SAFETYGLIDE¿ INSULIN SYRINGE WITH ATTACHED NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·January 29, 2020

    QUADRA-P FEMORAL STEMS

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·November 18, 2025

    SYRINGE 3ML LL W/NDL SFTYGLD 25X1 RB

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code MEG·March 7, 2019

    840 VENTILATOR

    FDA Adverse Event
    Injury ·COVIDIEN·Product code CBK·August 1, 2017

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code CBK·July 25, 2017

    BD SAFETYGLIDE NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMI·December 8, 2020

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code CBK·August 17, 2017