BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    DELTA FLOW

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MR 7700

    FDA UDI
    Philips Medical Systems Nederland B.V.·00884838115781·Upgrade to the MR 7700 gradient performance for...

    PORTABLE X-RAY SYSTEM, MODELS DIOX-602, PROX

    FDA 510(k)
    FDA Class 2 ·Dental

    The ICHOR Panacea Vascular Embolectomy Catheter System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LARGE NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·April 30, 2014

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 11, 2012

    INFUSOR LV5, 12 PK

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·August 3, 2010