BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    D.C. AMPLIFIER MODULE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GIRAFFE AND PANDA BAG AND MASK RESUSCITATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Lacriflow CL

    FDA 510(k)
    FDA Unclassified ·Unknown

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 10, 2014

    PINNACLE MTL INS NEUT40IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·October 3, 2012

    I-STAT CG8+ CARTRIDGE & I-STAT G3+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code CHL·July 20, 2010