BEUDAMED
    13 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    LL Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    N/A

    FDA UDI
    Medos International Sàrl·10886705032426·

    ANEMIAPRO SELF-SCREENER

    FDA 510(k)
    FDA Class 2 ·Hematology

    Passeo-35 PTA Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BIPOL LEAD MODEL 300

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code MUZ·November 11, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·September 10, 2011

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 23, 2013

    COBAS 6000 E 601 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·March 5, 2018

    ELECSYS FT3 III

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CDP·August 27, 2018

    ELECSYS FT3 III

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CDP·June 4, 2018

    ELECSYS FT3 III

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CDP·September 6, 2018

    ELECSYS FT3 III

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CDP·August 27, 2018

    ELECSYS FT3 III

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CDP·June 4, 2018