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 ×

    JOURNEY II XR Knee Instruments

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VERIFY BIOLOGICAL INDICATOR CHALLENGE PACK FOR VAPORIZED VH202 STERILIZATION PROCESSES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DVO EXTENDED ARTICULATION HUMERAL HEADS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    V 2.5 FIRM EXT

    FDA Adverse Event
    Injury ·CONCENTRIC MEDICAL·Product code NRY·June 17, 2013

    VITALITY 2

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 23, 2011

    COLLEAGUE VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 25, 2008