BEUDAMED
    11 results · 24ms · Sources: EU EUDAMED, US FDA

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    ARIX Ankle System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690127260·AK3 PS Insert Trial Size 6, 16mm

    V. MUELLER CAMERA CONTROLLER WITH STORAGE CART

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PINPOINT STEREOTACTIC HEAD AND NECK LOCALIZER

    FDA 510(k)
    FDA Class 2 ·Radiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

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

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code JDI·October 22, 2014

    RUSCH FOLEY CATHETER 2-WAY SILICONE 3CC 10FR

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code EZL·July 13, 2011

    MW5030686

    FDA Adverse Event
    Injury ·June 21, 2013

    Quanta System Sterile Optical Laser Fiber, single use

    FDA Enforcement
    Class II ·Terminated·Quanta System, S.p.A.·June 16, 2021

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·October 3, 2016

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·August 26, 2016