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

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    Fully Automatic Electronic Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CEMENTED HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304254206·

    ABLE CENTRAL VENOUS CATHETER

    FDA UDI
    Guangdong Baihe Medical Technology Co., Ltd.·06938634475175·

    VIEWRAY TREATMENT PLANNING AND DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    VERITAS COLLAGEN MATRIX

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

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·November 10, 2016

    IMPLANTABLE INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·November 11, 2016

    ADAPTA DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·October 10, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 15, 2011

    6000 CMS IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 13, 2013

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·November 10, 2016