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

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    PTFE Guidewire

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776166137·NORFOLK-NORWICH RETRACTOR PRONGS BLUNT

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·14026704920607·

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704266443·FRAZIER TUBE 7 FRENCH

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A242824120·24mm H x 28mm W x 24mm L x 12 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A24282480·24mm H x 28mm W x 24mm L x 8 Degree ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A242824150·24mm H x 28mm W x 24mm L x 15 degrees ALIF

    FREQUENCY 38 AND SILVER 07 (POLYMACON) SOFT (HYDROPHILIC) CONTACT LENS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    LX-100 Hair Growth Stimulation System

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 11, 2014

    RIATA ACTIVE FIXATION

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

    GYNECARE TVT ABBREVO CONTINENCE SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·July 23, 2013

    BD INSYTE AUTOGUARD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·January 30, 2025