BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    ONE-WAY VALVE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517360830·CoRoent SI Drill Bit, 2.0x12mm

    discovery®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011790151000·discovery® Bracket with hook, - 22° Torque, 0° ...

    APPLICATOR,ANGIOGRAPHY (7310MOBIN-UDDIN)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    COBRA Fusion Ablation System

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

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·May 26, 2021

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 5, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 15, 2012

    SCORPIO PS FEMUR WAFFLE W/LFIT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·August 3, 2010

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·May 26, 2021

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·October 1, 2019