BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    HUMIDIFIER-CASCADE II

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110577·COAXIAL IRRIGATING/ASPIRATING TIP CURVED

    NAVIAID BGE DEVICE, MODEL 21-001

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

    REDAPT Anteverted Cemented Liner

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 26, 2012

    OLYMPUS CAPSULE ENDOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code KOG·April 9, 2014

    GEMSTAR 7 THERAPY

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·July 14, 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