BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Co-Ablation System with Sterile Co-Ablation Probe

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

    AIRCAST

    FDA UDI
    DJO, LLC·00888912277815·VENAFLOW ELITE XL CALF CUFF - 20 PAIRS

    SonarMed AirWave, Airway Monitoring System

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PROCERA IMPLANT BRIDGE, MODELS 15-1001, 15-1002, 15-1051, 15-1052

    FDA 510(k)
    FDA Class 2 ·Dental

    ALINITY C CALCIUM2

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code CJY·March 5, 2026

    STYLE 120 SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·May 6, 2021

    STYLE 120 SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·May 6, 2021

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 11, 2011

    UNKNOWN DEPUY HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·November 21, 2008

    HIRES 90K ADVANTAGE IMPLANT

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS LLC·Product code MCM·July 18, 2013