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

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    Microcurrent device (Model: HBR2-1)

    FDA 510(k)
    FDA Class 2 ·Neurology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517297389·CoRoent® XLK, 10x18x55mm

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517286048·CoRoent® XL-CTW, 10x22x55mm

    PMT® Halo Systems

    FDA UDI
    PMT CORPORATION·00650551110804·HALO, 1203-5 VEST PED2, ACRYLIC LINER, 1211-1 X...

    Straight Compression Plate

    FDA UDI
    I.T.S. GmbH·09120034308529·Straight Compression Plate, 3.5mm, 5-Hole

    Sapphire Connect Power Supply

    FDA UDI
    EITAN MEDICAL LTD·17290109154494·

    THE O'NEIL STERILE FIELD URINARY CATHETER KIT WITH PREP PADS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    GALAXY SYSTEM; JUPITER

    FDA 510(k)
    FDA Class 2 ·Neurology

    TOTAL FEMUR

    FDA Adverse Event
    Injury ·STANMORE IMPLANTS WORLDWIDE·Product code KRO·June 7, 2018

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·October 20, 2022

    CUSTOM TOTAL FEMUR REPLACEMENT IMPLANT

    FDA Adverse Event
    Injury ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 24, 2014

    UNKNOWN SPINAL CORD STIMULATION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·October 24, 2008

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·August 5, 2011

    EASYTRAK 3

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code OJX·July 8, 2013

    CUSTOM TOTAL FEMUR REPLACEMENT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD·Product code JDI·July 24, 2015

    CUSTOM TOTAL FEMORAL REPLACEMENT IMPLANT

    FDA Adverse Event
    Injury ·STANMORE IMPLANTS WORLDWIDE LTD·Product code JDI·December 23, 2014

    CUSTOM TOTAL FEMUR REPLACEMENT IMPLANT

    FDA Adverse Event
    Injury ·STANMORE IMPLANTS WORLDWIDE LTD·Product code KRO·December 1, 2014

    PROXIMAL FEMUR

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD·Product code JDI·December 23, 2014

    PATIENT SPECIFIC TOTAL FEMUR

    FDA Adverse Event
    Injury ·STANMORE IMPLANTS WORLDWIDE·Product code KRO·August 15, 2018

    FEM KNEE W/EPI R SM

    FDA Adverse Event
    Injury ·STANMORE IMPLANTS WORLDWIDE·Product code KRO·January 16, 2020