BEUDAMED
    11 results · 32ms · Sources: EU EUDAMED, US FDA

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    HYGEIA URINE PREGNANCY TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Modulus

    FDA UDI
    Nuvasive, Inc.·00887517024138·Modulus ALIF Trial, 12x42x32mm 20° XL

    BOUNDARY SINGLE-USE DRAPES

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

    INFRARED EAR THERMOMETER, MODEL ET-101A

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·June 29, 2023

    HELICAL BLADE COUPLING SCREW

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code LXH·June 18, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·October 25, 2010

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·December 20, 2012

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·June 30, 2023

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·September 1, 2017

    ESSURE

    FDA Adverse Event
    Malfunction ·BAYER PHARMA AG·Product code HHS·May 1, 2017