BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    REGULATOR FLOWMETER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    MATIRA ANTERIOR CERVICAL SYSTEM

    FDA UDI
    Kalitec Direct LLC·B07307K0155050·Trial, Drill Guide, 15 x 12, 5mm, Tapered

    OrthoGrid Hip AI

    FDA UDI
    Orthogrid Systems, Inc.·00860003424834·OrthoGrid Hip AI for non-invasive software syst...

    VAS-CATH URETERAL STENTS CATHETER, MODIFICATION

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

    FIXATION WIRE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·PURITAN BENNET CORP·Product code CBK·November 5, 2010

    SETROX S 53

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·January 9, 2013

    SITTER ELITE

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code KMI·February 25, 2014