BEUDAMED
    33 results · 25ms · Sources: EU EUDAMED, US FDA

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    MICROLIFE DIGITAL UNDERARM THERMOMETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RINGLOC HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304230033·

    WELCH ALLYN SPOT VITAL SIGNS LXI MODEL 45000 SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CARBODISSECTING ENDOSCOPE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    OT VERIO TEST STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 9, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 19, 2014

    HYDROCOIL 14-SYSTEM DETACHABLE COIL (HES)

    FDA Adverse Event
    Injury ·MICROVENTION, INC.·Product code HCG·May 23, 2011

    UNKNOWN CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·September 22, 2017

    M2A-MAGNUM 42-50M TPR INSRT +3

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 21, 2017

    M2A-MAGNUM MOD HD SZ 46MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 21, 2017

    UNKNOWN STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·July 21, 2017

    AQUACEL FOAM

    FDA Adverse Event
    Malfunction ·CONVATEC LTD·Product code NAC·November 17, 2025

    MICRUSFRAME10 5MM X 17CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 15, 2022

    GALAXY G3 XSFT 4MM X 10CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 15, 2022

    GALAXY G3 XSFT 4MM X 10CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 15, 2022

    GALAXY G3 XSFT 2.5MM X 3.5CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 15, 2022

    GALAXY G3 XSFT 3MM X 8CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 15, 2022

    I-STAT CHEM8+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JPI·December 17, 2024

    ANTEGRADE FEM CONNECTING BOLT

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LXH·November 11, 2017

    MICRUSFRAME10 6MM X 11.9CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 7, 2022