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

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    ROCHE COBAS AMPLICOR ANALYZER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MICROSPAN SYSTEM

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code FED·June 8, 2006

    SPACELABS - ARRHYTHMIA NET (TM) LEVEL 1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACTIVE ADAPTER

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

    UNKNOWN PRODUCT - SET SCREW

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HWC·October 12, 2012

    XENIUM XPM

    FDA Adverse Event
    Malfunction ·NIPRO CORPORATION *USD*·Product code KDI·February 15, 2013

    LD304 MATERNITY BED

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code HDD·December 22, 2010

    IMMERSION HYDROBATH

    FDA Adverse Event
    Malfunction ·INVACARE CLEVELAND STREET·Product code ILJ·July 29, 2014