BEUDAMED
    9 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.

    SMALL VESSEL CANNULA

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772412501·PROTECT.LUMBOSTYLE BACK SUPPORT BLACK IV

    Ortho Specialties

    FDA UDI
    Young Innovations, Inc.·00843471186916·Bicuspid Bands, Lower, Size 24

    ULTRAZYME ALKALINE PHOSPHATASE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MARATHON STENT WITH FUSION TECHNOLOGY

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·September 26, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·December 19, 2013

    XIA BLOCKER

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code NKB·July 9, 2010

    Heritage Labs Appraise A1c Diabetes Home Test , Product K7609, 24 kits/shipping carton (Product K7609), each kit packed in a box and contains 1 Triad Medium Alcohol Prep Pad, Cat. No. 10-3001, NDC 50730-3001-0, and blood specimen collection supplies, forms, and instructions Blood specimen collection

    FDA Recall
    Terminated ·Heritage Labs International LLC·Product code LCP·January 9, 2011