BEUDAMED
    12 results · 17ms · Sources: EU EUDAMED, US FDA

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    B.G. FLEXIBLE NAIL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Sherlock

    FDA UDI
    Bard Access Systems, Inc.·00801741124358·SHERLOCK 3CG TCS DISPLAY

    ELMED INCORPORATED

    FDA UDI
    ELMED INCORPORATED·00198506082870·NASAL CUTTING FORCEPS, SINGLE ACTION STRAIGHT J...

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209137282·

    The Orthodontic Store

    FDA UDI
    Young Innovations, Inc.·00843471182635·.022 U/L Std. Weld Size #30

    Drive

    FDA UDI
    Drive Devilbiss Healthcare·00775757701301·Walkers, All Types1-Button Product Description:...

    ORBITAL RECONSTRUCTIVE IMPLANT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Dynamic Coronary Roadmap

    FDA 510(k)
    FDA Class 2 ·Radiology

    DEXTRUS 4135

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVN·April 24, 2014

    ASR UNI FEMORAL IMPL SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code JDI·October 3, 2012

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 20, 2010

    Armada 35/ Armada 35 LL PTA Catheters. The device is intended for dilatation of lesions in the vasculature.

    FDA Enforcement
    Class II ·Terminated·Abbott Vascular·October 3, 2012