BEUDAMED
    9 results · 24ms · Sources: EU EUDAMED, US FDA

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    POWERPORT CLEARVUE SLIM IMPLANTABLE PORT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970546·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970553·

    ARTHREX BIO-SUTURE

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

    PHILIPS INTEGRIS ALLURA FLAT DETECTOR RELEASE 1.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    ACCUSTICK II

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code DYB·August 17, 2007

    ACCU-CHEK ® SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE AG·Product code LZG·May 21, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 26, 2014

    ENRHYTHM DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·June 14, 2011