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

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    GOLDSMITH & REVERE TENARY ALLOY

    FDA 510(k)
    FDA Class 2 ·Dental

    TREK OTW CORONARY DILATATION CATHETER MINI TREK OTW CORONARY DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LAD, MODEL LAD-01

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 16, 2014

    MINICAP TRANSFER SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·November 6, 2012

    CAUTERY PENCIL PUSHBUTTON

    FDA Adverse Event
    Other ·MEDLINE INDUSTRIES, INC.·Product code GEI·August 26, 2010

    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