BEUDAMED
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    UREA NITROGEN (BUN) LIQUID REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981106·anteriors; shade A3.5; mould UM6

    Cabo™

    FDA UDI
    NEUROSTRUCTURES, INC·00841508104193·Fixed Screw Caddy

    Powder Free Nitrile Patient Examination Gloves, Blue Color

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PERI-LOC PERIARTICULAR LOCKED PLATING SYSTEM VOLAR DISTAL RADIUS LOCKING PLATE FOR THE UPPER EXTREMITY-ASTM F139

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ETEST FOSFOMYCIN FM 1024 WW B30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code JWY·April 16, 2020

    ALARIS PUMP MODULE IV ADMINISTRATION SET

    FDA Adverse Event
    Injury ·CAREFUSION CORPORATION·Product code FPA·February 20, 2013

    PUMP,COLLEAGUE SINGLE CHANNELCOLOUR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·February 8, 2011

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Death ·BAXTER HEATHCARE CORPORATION·Product code FKX·August 5, 2014

    WHITESTAR PHACO HANDPIECE

    FDA Adverse Event
    Malfunction ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HQC·July 31, 2024