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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    NIDEK MODEL YC-1200

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    GYC-1000

    FDA Adverse Event
    Malfunction ·NIDEK CO., LTD.·Product code HQF·June 18, 2015

    IMMULITE 2000 3G ALLERGY SPECIFIC IGE ASSAY KIT MODEL L2KUN6

    FDA 510(k)
    FDA Class 2 ·Immunology

    PYR BROTH

    FDA 510(k)
    FDA Class 1 ·Microbiology

    ULTHERA

    FDA Adverse Event
    Injury ·ULTHERA INC.·Product code OHV·June 10, 2014

    KEEPSAFE FALL MONITOR

    FDA Adverse Event
    Malfunction ·DONGGUAN POSEY MEDICAL DEVICE LTD.·Product code KMI·November 3, 2010

    OBTAPE TRANSOBTURATOR SLING

    FDA Adverse Event
    Injury ·MENTOR WORLDWIDE LLC·Product code FTL·December 21, 2012