BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    NormaTec Pulse and NormaTec Pulse Pro

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    GEN4 Direct Access

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828185639·GEN4 Direct Access

    ENDOSCOPIC APPLICATOR

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

    SEVOFLURANE VAPORIZER ADAPTOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·March 28, 2017

    MOTORIZED 3-WHEELED VEHICLE FOR OUTSIDE TRANSPORT

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code INI·June 10, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·June 30, 2011

    ETS FLEX ARTICNG LNR CUTR 45MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code GDW·September 5, 2008

    13 CM TRICUT BLADE

    FDA Adverse Event
    Malfunction ·MEDTRONIC ENT (JACKSONVILLE)·Product code HAW·July 23, 2015

    CURVED SINUS BURS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EQJ·June 2, 2014

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·July 4, 2016