BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    IMMUNOGLOBULIN A TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    JEDMED

    FDA UDI
    JEDMED INSTRUMENT COMPANY·M6339905520·INSTRUMENT TRAY W/O COVER 10"X6-1/2

    JJ Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    UROCARE

    FDA 510(k)
    FDA Class 2 ·Radiology

    COULTER® ACT DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC·Product code GKZ·December 7, 2010

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    UNKNOWN·Product code ITJ·March 5, 2013

    REVEAL XT

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code DSI·February 15, 2011

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC MILACA, INC.·Product code LWP·August 8, 2014