BEUDAMED
    26 results · 23ms · Sources: EU EUDAMED, US FDA

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    DISPOSABLE POWDERED VINYL EXAM GLOVE, YELLOW COLOR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16710711220·

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771048999·K-Wires, Double trocar, .045-inch (1.1mm) diame...

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704292640·

    Key Surgical K-Wires and Steinmann Pins

    FDA UDI
    KEY SURGICAL, INC.·00849771012412·K-Wires, Double trocar, .045-inch (1.1mm) diame...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587P07112270·7mm PLIF Implant 11mm Wide 22mm Length, 7 deg L...

    BALLPEN SPINAL NEEDLE W/WO INTRODUCER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PROLENE SOFT (POLYPROPYLENE), NONABSORBABALE SYNTHETIC SURGICAL MESH

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

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 22, 2013

    ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA·Product code MCX·April 27, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 10, 2008

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DXY·April 15, 2019

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DXY·April 15, 2019

    UNK KNEE TIBIAL TRAY LCS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code NJL·January 28, 2021

    UNK KNEE FEMORAL LCS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code NJL·January 28, 2021

    UNK KNEE TIBIAL INSERT LCS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code NJL·January 28, 2021

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 15, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 11, 2017