BEUDAMED
    9 results · 34ms · Sources: EU EUDAMED, US FDA

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    DUO-LITE PHOTOTHERAPY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GDC POWER SUPPLY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - FREMONT·Product code HCG·July 20, 2010

    SYNCHRON URIC ACID

    FDA Adverse Event
    BECKMAN COULTER INC.·Product code KNK·June 10, 2011

    GAS CHROMATOGRAPH

    FDA 510(k)

    Quingo Flyte Mobility Scooter

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    VACUETTE BLOOD COLLECTION TUBE 3ML K2E K2EDTA

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NA INC.·Product code JKA·November 2, 2020

    SCREW CORTEX

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWP·February 21, 2013

    22MM COCR RADIAL HEAD STANDARD HEIGHT/12.5MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWI·July 31, 2014

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 26, 2011