BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Occlusion Balloon Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AXIS PACS, HMS PACS

    FDA 510(k)
    FDA Class 2 ·Radiology

    UROVAL BRS SYSTEM, MODEL BRS01; TELESIS, MODEL PROMO1

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    UNKNOWN HARRIS/GALANTE FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code KWZ·March 1, 2016

    UNKNOWN HARRIS/GALANTE FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code KWZ·March 1, 2016

    FLO-GARD 6301 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FRN·October 4, 2008

    M2A-MAGNUM MODULAR HEAD SIZE 46MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 22, 2013

    UNICEL DXC 600 SYNCHRON CLINICAL SYSTEM

    FDA Adverse Event
    Injury ·BECKMAN COULTER, INC.·Product code JGS·July 22, 2011