BEUDAMED
    13 results · 19ms · Sources: EU EUDAMED, US FDA

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    BURRON PERCUTANEOUS INDUCER SET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Custom Healthcare Systems Inc.

    FDA UDI
    Manus Medical, LLC·00811870030055·

    Cabo™

    FDA UDI
    NEUROSTRUCTURES, INC·00841508101536·4 LEVEL PLATE 60mm

    LIFELINES TRACKIT

    FDA 510(k)
    FDA Class 2 ·Neurology

    Theradome LH40

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172972113·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971604·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971611·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172973585·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172972106·

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 15, 2014

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 31, 2012

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 2, 2015