BEUDAMED
    7 results · 25ms · Sources: EU EUDAMED, US FDA

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    ERGOMAT 8000 SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122772·K-WIRE - SINGLE TROCAR THREADED 2.0mm DIA x 230mm

    Resection Electrodes

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    RPS ADENO DETECTOR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·February 9, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·January 7, 2011

    UNKNOWN

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code HRS·July 23, 2014