BEUDAMED
    6 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.

    MODIFIED LASERFLO BLOOD PERFUSION MONITOR, BPM403A

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPECTACLE FRAMES VARIOUS COLORS AND DESIGNS

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    TRANSFER-TRAX (TM) SPLINT TRACTION

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    MOSAIC AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·HEART VALVES SANTA ANA·Product code LWR·June 16, 2014

    *

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code JDR·October 9, 2012

    ACCUSOL 35 5000ML (DRUG) (UK,IRELAND,POLAND,CZECH REP.,SLOV

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CASTLEBAR·Product code KPO·October 19, 2010