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

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    MENISCUS CHIN IMPLANT

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

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704267396·

    AUTOVAC (R) AUTOTRANSFUSION SYSTEM, 7900 MODIFIED

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    REACTIFS, IBF ULTROGELS ACA & ULTROGELS A

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SPIROBAC FILTER REINF MEMBRANE

    FDA Adverse Event
    Malfunction ·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code CAH·August 1, 2012

    VERSASAFE SPLIT SEPTUM SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FPA·May 7, 2014

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·February 5, 2013

    PEG DRIVER 2.0MM FAST

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·December 6, 2010

    SINGLE USE PAPER FILTER WITH INDICATOR

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code FRG·January 30, 2019