BEUDAMED
    6 results · 19ms · 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.
    Filters Regulation: Us FDA ×

    QUALTEX NEEDLE COUNTERS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    FUNCTIONAL BRAIN MAPPING OPTION FOR MRI

    FDA 510(k)
    FDA Class 2 ·Radiology

    ALIMAXX-B UNCOVERED BILIARY STENT SYSTEM ENDOSCOPIC

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

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 30, 2014

    CARPENTIER-EDWARDS PERIMOUNT THEON PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·November 20, 2010

    LUMAX 340 DR-T

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code MRM·November 29, 2012