BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    ELECTRONIC INSUFFLATOR, MODEL NO. 2054.60

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Modulus

    FDA UDI
    Nuvasive, Inc.·00887517024060·Modulus ALIF Trial, 6x42x32mm 15° XL

    ARTERIAL BLOOD SAMPLING KIT

    FDA 510(k)
    FDA Class 1 ·General Hospital

    GE LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS 5205000, 5205000-2

    FDA 510(k)
    FDA Class 2 ·Radiology

    TI 12-POINT NUT-11MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·June 18, 2014

    INTEGRATED APD SET W/CASSETTE3-PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·October 25, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·December 20, 2012

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·September 11, 2019

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·May 13, 2020