BEUDAMED
    9 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    SPIROBAC ADAPTERS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SPIROBAC FILTER REINF MEMBRANE

    FDA Adverse Event
    Malfunction ·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code CAH·August 1, 2012

    TOSHIBA DIGITAL CLINICAL THERMOMETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PHILIPS MULTILEAF COLLIMATOR (MLC)

    FDA 510(k)
    FDA Class 2 ·Radiology

    DEPUY ASR XL FEM IMP SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.·Product code KWA·February 5, 2013

    ISERT ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS INC.·Product code HQL·December 6, 2010

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·July 18, 2014

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·June 25, 2019

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·January 14, 2020