BEUDAMED
    12 results · 22ms · Sources: EU EUDAMED, US FDA

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    R.R.P.S. RADIUS RECONSTRUTION PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Turbo-Flo PICC Sets

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SAS LEGIONELLA TEST, SAS LEGIONELLA DIPSTICK TEST

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SINGLE LUMEN PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LJS·December 19, 2017

    ARTICUL/EZE M 36MM +5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. REG. # 8010379·Product code JDI·February 14, 2013

    BHR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code NXT·July 28, 2014

    ACS HI-TORQUE BALANCE MIDDLEWEIGHT GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATIN

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code DQX·January 14, 2011

    TURBO-FLO SINGLE LUMEN CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·October 1, 2018

    TURBO-FLO SINGLE LUMEN CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·October 1, 2018

    ELECSYS TSH ASSAY

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JLW·November 9, 2020

    FT4, FREE THYROXINE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEC·September 30, 2016

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Injury ·COOK INC·Product code FAD·March 26, 2018