BEUDAMED
    31 results · 28ms · Sources: EU EUDAMED, US FDA

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    WALLSTENT TRACHEOBRONCHIAL PROSTHESIS MODIFICATION

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

    SwishTapered™ Implant

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307106432·4.1mmD x 16mmL, 4.8mmD Platform

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471129443·K-WIRE - DOUBLE TROCAR WITH GUIDE 1.1mm DIA x 1...

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122970·K-WIRE - SINGLE TROCAR 1.1mm DIA x 150mm

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867059986·ARTHREX ECLIPSE HUMERAL HEAD, 41/16

    DEAE-DEXTRAN IN PBS

    FDA 510(k)
    FDA Class 1 ·Hematology

    Trigon Trigon HA Stand-Alone Wedge Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNIVERSAL GLENOID - CENTRAL SCREW 20MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·February 26, 2024

    FREESTYLE LITE

    FDA Adverse Event
    Malfunction ·Product code NBW·April 6, 2010

    ECLIPSE CAGE SCREW S, 30MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code QHQ·December 16, 2019

    ARTHREX ECLIPSE HUMERAL HEAD, 41/16

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code QHQ·December 16, 2019

    ECLIPSE TRUNION,41 MM TPS CTD

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code QHQ·December 16, 2019

    ARTHREX ECLIPSE HUMERAL HEAD, 41/16

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code QHQ·January 23, 2023

    ECLIPSE CAGE SCREW M, 35MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code QHQ·January 23, 2023

    UNIVERS VAULTLOCK GLENOID, SMALL

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·January 23, 2023

    ARTHREX ECLIPSE HUMERAL HEAD, 41/16

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code QHQ·December 4, 2019

    ECLIPSE TRUNION,41 MM TPS CTD

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code QHQ·December 4, 2019

    ECLIPSE CAGE SCREW S, 30MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code QHQ·December 4, 2019

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 3, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 1, 2014