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

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    MICROWAVE AUTOMATED TISSUE PROCESSOR

    FDA 510(k)
    FDA Class 1 ·Pathology

    OHMEDA MODEL 5250 RGM MONITOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    KODAK EKTASCAN LASER PRINTER, MODEL 100 XLP

    FDA 510(k)
    FDA Class 2 ·Radiology

    NA

    FDA UDI
    STERILMED, INC.·10888551007580·SAW BLADE SAGITTAL K9 K2000 SERIES

    NA

    FDA UDI
    STERILMED, INC.·10888551007573·SAW BLADE SAGITTAL FLARED K9 K2000 SERIES

    NA

    FDA UDI
    STERILMED, INC.·10888551007559·SAW BLADE SAGITTAL K9 K2000 SERIES

    NA

    FDA UDI
    STERILMED, INC.·10888551007566·SAW BLADE SAGITTAL K9 K2000 SERIES

    NA

    FDA UDI
    STERILMED, INC.·10888551007603·SAW BLADE SAGITTAL K9 K2000 SERIES

    NA

    FDA UDI
    STERILMED, INC.·10888551007597·SAW BLADE SAGITTAL K9 K2000 SERIES

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·January 22, 2013

    KAPPA 900 DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·December 14, 2010

    OT VERIO SYNC METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 10, 2014