BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    BAXTER HANDLE MODEL 1150

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    COMPARTMENT SYNDROME PRESSURE MONITOR SYS

    FDA 510(k)
    FDA Unclassified ·Unknown

    ECLIPSE 2100(TM) MODEL 32

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

    EXTENSION SET 30IN

    FDA Adverse Event
    Malfunction ·HOSPIRA INC.·Product code FPA·June 3, 2009

    SPIROBAC FILTER REINF MEMBRANE

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

    APM/AIM PUMP SET W/C

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·September 28, 2010

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·January 9, 2013

    ECHELON*FLEX60

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code GDW·January 3, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 18, 2014

    TM-ECOCHGTRODE

    FDA Adverse Event
    Other ·NATUS MEDICAL INC·Product code GXY·January 9, 2009