BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    VITEK GRAM POSITIVE IDENTIFICATION CARD (GPI)

    FDA 510(k)
    FDA Class 1 ·Microbiology

    De Soutter Medical

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

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123113·K-WIRE - DOUBLE TROCAR 0.9mm DIA x 125mm

    Ultraviolet Lamps Intended for Use in Sunlamp Products (commonly known as metal halide sunlamps)

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

    MODIFICATION TO: DIRECT DIGITIZER REGIUS MODEL 190

    FDA 510(k)
    FDA Class 2 ·Radiology

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code NIK·February 9, 2013

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 23, 2014

    FINELINE II

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