BEUDAMED
    54 results · 22ms · Sources: EU EUDAMED, US FDA

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    reVive Light Therapy LED Ultrasonic Wrinkle System

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

    BI-METRIC XR-SERIES HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304650701·

    BI-METRIC XR-SERIES HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304650350·

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197453165·CCR Titanium Medial Blade 24x45m...

    All Poly Keel Drill

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215063955·

    LION SE ONE STEP ORTHODONTIC ADHESIVE

    FDA 510(k)
    FDA Class 2 ·Dental

    KLASSIC HD HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD PRECISIONGLIDE NEEDLE 18G 1 1/2IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMI·July 25, 2023

    INSPIRE 8F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·May 5, 2020

    INSPIRE 8F M

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·January 3, 2024

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 20, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 27, 2011

    PHILLIPS

    FDA Adverse Event
    Injury ·PHILLIPS HEALTHCARE·Product code CBK·September 23, 2008

    INSPIRE 8F M

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA·Product code DTZ·January 4, 2024

    INSPIRE OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·March 12, 2026

    INSPIRE OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·March 12, 2026

    INSPIRE 8F

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA·Product code DTZ·November 5, 2025

    INSPIRE 8F

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA·Product code DTZ·November 5, 2025

    INSPIRE OXYGENATOR

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA·Product code DTZ·December 11, 2025

    INSPIRE 8F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·April 20, 2021