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

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    MODULAR BIOPSY FORCEP

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704269260·

    M2A-MAGNUM PF CUP 50ODX44ID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·June 18, 2018

    M2A-MAGNUM MOD HD SZ 44MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·June 18, 2018

    GLUCOFILM TEST STRIPS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    AUROLITE 85

    FDA 510(k)
    FDA Class 2 ·Dental

    RF GEN OBSOLETE REPLACED BY 0406900000

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code GXD·February 6, 2013

    HOMECHOICE CYCLER-REFURBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 4, 2011

    NEXGEN CRUCIATE RETAINING FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·July 10, 2014