BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    KSEA RIGID CULDOSCOPE AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Arthrex®

    FDA UDI
    ARTHREX, INC.·10888867400617·Calibrated measurement wire 1.1mm

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code HET·June 8, 2006

    LATEX EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    NUVASIVE HELIX REVOLUTION ACP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARCOM 28MM RNGLOC LINER HWALL 24

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·March 8, 2013

    ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·February 11, 2011

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·August 8, 2014

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·December 26, 2024

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·December 26, 2024