BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    DRAGER DVE 8080/81/82 WITH DVE 4002 OR DVE 4001 SERIES SYSTEM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    URETEX SUPPORT PP TRANSOBTUR2 KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code FTL·November 28, 2011

    URYXXON RELAX URINE ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Aequalis PerFORM Reversed, Aequalis PerFORM+ Reversed Glenoid

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EMERALD

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL OPTICS·Product code KYB·July 6, 2016

    S-ROM M HEAD 36MM +0

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·February 14, 2013

    CELL-DYN SAPPHIRE ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·January 14, 2011

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code LWS·July 28, 2014