BEUDAMED
    78 results · 37ms · Sources: EU EUDAMED, US FDA

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    Myoject Luer Lock Needle Electrode

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741614300·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674161430060·

    Oticon

    FDA UDI
    Oticon A/S·05707131305336·SENSEI PRO SP, BTE 13 WL 110 AQM TAR

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1614300·16mm H x 14mm W x 30mm L x 0 degrees XLIF

    Kirwan

    FDA UDI
    KIRWAN SURGICAL PRODUCTS LLC·00841019108413·Reusable TPR Bipolar Forceps 9" (22.9cm) Hardy ...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X16143080·16mm H x 14mm W x 30mm L x 8 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X161430120·16mm H x 14mm W x 30mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L161430120·16mm H x 14mm W x 30mm L XLIF Trial 12 degree L...

    OneCath

    FDA UDI
    COMPACTCATH, INC.·00852141007475·The OneCath Intermittent Urinary Catheter is a ...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523137992·Trial, 30 X 26, 15mm Height 22° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138012·Trial, 30 X 26, 19mm Height 22° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138005·Trial, 30 X 26, 17mm Height 22° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523137985·Trial, 30 X 26, 13mm Height 22° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138029·Trial, 30 X 26, 21mm Height 22° Hyperlordotic

    MLS-AC DERMA SCANNER

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SYSTEM 83 PLUS MINIFLEX WASHER-DISINFECTOR

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

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 11, 2021

    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