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

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    ENA SCREEN ELISA TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    PowerPumpTM dp System Patient tubing

    FDA UDI
    INSIGHTRA MEDICAL, INC.·17350021986143·

    VARIAX

    FDA UDI
    Stryker GmbH·07613327615463·Volar Distal Radius Plate Insert, Right

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150720·K-WIRE - SINGLE TROCAR 1.1mm DIA x 100mm

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150713·K-WIRE - SINGLE TROCAR 1.0mm DIA x 100mm

    Biomet Kirschner Wires (K-Wires)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TSH-CTK-3 IRMA

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    EXTENSION SET 30IN

    FDA Adverse Event
    Malfunction ·HOSPIRA INC.·Product code FPA·June 3, 2009

    APM/AIM PUMP SET W/C

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·September 28, 2010

    LIFEPAK CR PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·December 8, 2010

    EDWARDS SAPIEN TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·July 17, 2014

    CAUTERY UNIT

    FDA Adverse Event
    Malfunction ·PENTAX MEDICAL CO.·Product code FDF·October 17, 2006