BEUDAMED
    15 results · 32ms · Sources: EU EUDAMED, US FDA

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    VB-1830/VB-1530, VIDEO BRONCHOSCOPE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Iris Retractor

    FDA UDI
    KATENA PRODUCTS, INC.·00841668103708·GRAETHER IRIS RETRACTOR W/ IRRIGATOR STR

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867060074·ARTHREX ECLIPSE HUMERAL HEAD, 49/20

    BIOFEEDBACK SYSTEM/3

    FDA 510(k)
    FDA Class 2 ·Neurology

    AMBU MATIC AUTOMATIC RESUSCITATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    UNKNOWN MENTOR

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·September 21, 2023

    UNKNOWN MENTOR

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·September 21, 2023

    NATURALYTE

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 23, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 4, 2013

    COULTER ® LH750

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code GKZ·December 21, 2010

    GLENOID, POLY WITH KEEL, LARGE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·August 13, 2019

    ARTHREX ECLIPSE HUMERAL HEAD, 49/18

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code QHQ·July 28, 2020

    UNIVERSAL GLENOID - INLAY LARGE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·April 30, 2019

    UNK

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code QHQ·December 31, 2025

    ARTHREX ECLIPSE HUMERAL HEAD, 49/18

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code QHQ·December 31, 2025