BEUDAMED
    6 results · 19ms · 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 ×

    COSGROVE DEPTH ELECTRODE KIT(CDEK)

    FDA 510(k)
    FDA Class 2 ·Neurology

    MODIFIED LABELING FOR ACA LIPASE ANALYTICAL TEST

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    VAGINAL CHAMBER PELLETHANE-MEDICAL GRADE 2363

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SM204 M-SERIES W/BIG WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·February 14, 2013

    HOMECHOICE PROAUTOMATED PD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·July 28, 2014

    PROPOSED TRADEMAN MICROVASIVE POLYPECTOMY SNARES

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code FDI·January 14, 2011