BEUDAMED
    7 results · 24ms · Sources: EU EUDAMED, US FDA

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    Electric Handpiece Motor

    FDA 510(k)
    FDA Class 1 ·Dental

    RETCAM 3 OPHTHALMIC IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PEDIATRIC HEAD-SPINE COIL (MODEL:5000012701

    FDA 510(k)
    FDA Class 2 ·Radiology

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·June 21, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011

    GE OEC 9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 19, 2008

    Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator.

    FDA Enforcement
    Class II ·Terminated·Philips North America, LLC·March 25, 2020