BEUDAMED
    73 results · 27ms · Sources: EU EUDAMED, US FDA

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    VARIAX DISTAL RADIUS PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741414300·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674141430060·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1414300·14mm H x 14mm W x 30mm L x 0 degrees XLIF

    UHF22 Transducer

    FDA UDI
    FUJIFILM SONOSITE, INC.·00841517102302·Diagnostic Ultrasound Transducer

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L141430120·14mm H x 14mm W x 30mm L XLIF Trial 12 degree L...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X141430120·14mm H x 14mm W x 30mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X14143080·14mm H x 14mm W x 30mm L x 8 degrees XLIF

    Chic

    FDA UDI
    Gc Orthodontics America Inc.·D78814143000101·CHIC ROTH 018/LR3 -11T 7A 2M

    Chic

    FDA UDI
    Gc Orthodontics America Inc.·E53514143000101·CHIC ROTH 018/LR3 -11T 7A 2M

    K2M General Instruments

    FDA UDI
    VB Spine LLC·10888857581258·Split Tube Retractor Ø16x120 mm

    MLS-AC DERMA SCANNER

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BLEASE SIRIUS ANESTHESIA SYSTEM, MODELS 3000 AND 2000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·August 8, 2016

    EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·January 3, 2017

    EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·February 2, 2016

    EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FGE·September 27, 2016

    FGE CATHETER, BILIARY, DIAGNOSTIC - BILIARY STENT - METAL

    FDA Adverse Event
    Injury ·COOK INC·Product code FGE·January 29, 2020

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    GOBED+

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·June 1, 2011