BEUDAMED
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    ULTIMA RESPIRATORY EFFORT SENSOR MODELS 0520 AND 0522

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PE/Dazzle™ 594 anti-human CD10

    FDA UDI
    BIOLEGEND, INC.·00810034702692·URL: https://www.biolegend.com/en-us/products/p...

    TBD ETHICON MESH

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Merit Syringe

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CONTINU-FLO SOLN. SET, 3 LUERACTIVATED VALVES

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code FPA·February 9, 2011

    UNICEL DXH 800 COULTER CELLULAR ANALYSIS SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·August 5, 2014

    ABC E-PLATE INSERT FOR FJ885R & FJ889R

    FDA Adverse Event
    Malfunction ·AESCULAP, INC.·Product code KWQ·November 17, 2006