BEUDAMED
    7 results · 26ms · 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 ×

    ELECSYS FERRITIN

    FDA 510(k)
    FDA Class 2 ·Immunology

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704294217·

    MOSAIC DEVICES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Digital Blood Pressure Monitor-Wrist Style

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKNOWN ZIMMER KNEE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·February 19, 2013

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 27, 2011

    ALAIR?

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC - CORK·Product code OOY·July 31, 2014