BEUDAMED
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    uDR 780i

    FDA 510(k)
    FDA Class 2 ·Radiology

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704265279·

    NA

    FDA UDI
    SYNTHES (U.S.A.) LP·10886982165671·3.5MM CLAVICLE HOOK PLATE 8 HOLES RIGHT-18MM HO...

    2.0/2.4MM FRACTURE SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036036010·

    HEATED HUMIDIFIED SMOKE EVACUATION TUBE SET

    FDA Adverse Event
    Malfunction ·W.O.M. WORLD OF MEDICINE GMBH·Product code OSV·May 9, 2025

    ZEISS CATARACT SUITE MARKERLESS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    WEST NILE VIRUS IGG INDIRECT ELISA

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SPUR II

    FDA Adverse Event
    Malfunction ·AMBU, INC·Product code BTM·April 23, 2010

    PUMP MMT-715LNAS PRDGM INS V2.1 SK EN

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·November 21, 2008

    GYNECARE TVT OBURATOR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·July 22, 2013