BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    DYNAFEED

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    E-Z Tie Tubing

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746147920·ELASTOMERIC E-Z TIE TUBING 025 TRANSPARENT 25'

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209127061·

    MINI-1 TRANSCUTANEOUS ELEC-NERVE STIM

    FDA 510(k)
    FDA Class 2 ·Neurology

    Arthrex Beaming System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DELTEC GRIPPER PLUS POWER PAC

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC·Product code FPA·January 23, 2020

    MICROFRANCE®

    FDA Adverse Event
    Injury ·XOMED MICROFRANCE MFG·Product code GEI·June 6, 2014

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·December 3, 2012

    MAYFIELD INFINITY SKULL CLAMP

    FDA Adverse Event
    Malfunction ·INTEGRA-OHIO·Product code HBL·September 3, 2010