BEUDAMED
    27 results · 30ms · Sources: EU EUDAMED, US FDA

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    Self-destruction Safety Syringes for Single Use; Sterile Hypodermic Syringes for Single Use; Sterile Hypodermic Needles for Single Use; Sterile Safety Hypodermic Needles for Single Use

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Maestro™ Total Wrist

    FDA UDI
    Biomet Orthopedics, LLC·00887868239953·

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486000523·MCK Patellofemoral Component

    MAESTRO TOTAL WRIST

    FDA UDI
    Biomet Orthopedics, LLC·00880304555112·

    AUDIFON SUENO CIC, AUDIFON SUENO S, AUDIFON SUENO T CIC, AUDIFON SUENO T S

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    XKNIFE 5

    FDA 510(k)
    FDA Class 2 ·Radiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 11, 2025

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 30, 2026

    PRECICE STRYDE SYSTEM

    FDA Adverse Event
    Malfunction ·NUVASIVE SPECIALIZED ORTHOPEDICS, INC.·Product code HSB·May 26, 2021

    MED-EL MAESTRO COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·October 15, 2014

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011

    GYNECARE TVT RETROPUBIC SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·June 20, 2013

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 29, 2026

    BIO-MEDICUS NG 21 FR ARTERIAL CANNULA

    FDA Adverse Event
    Injury ·PERFUSION SYSTEMS·Product code DWF·October 19, 2018

    BIO-MEDICUS NG 17 FR ARTERIAL CANNULA

    FDA Adverse Event
    Injury ·PERFUSION SYSTEMS·Product code DWF·October 19, 2018

    BIO-MEDICUS NG 17 FR ARTERIAL CANNULA

    FDA Adverse Event
    Injury ·PERFUSION SYSTEMS·Product code DWF·October 19, 2018

    BIO-MEDICUS NG 15 FR ARTERIAL CANNULA

    FDA Adverse Event
    Injury ·PERFUSION SYSTEMS·Product code DWF·October 19, 2018

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 26, 2025

    TERUMO RADIFOCUS GUIDE WIRE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 3, 2025

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 21, 2018