BEUDAMED
    12 results · 22ms · Sources: EU EUDAMED, US FDA

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    EXTENDED USE ALDAHOL HIGH LEVEL DISINFECTANT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MICTEC KNOT PUSHER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09920918900·MICTEC KNOT PUSHER

    MICTEC KNOT PUSHER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896008007·MICTEC KNOT PUSHER

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450630334·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450325049·

    WAVEWRITER ALPHA 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·March 7, 2025

    G-2 VERSION 3, MODEL 10049

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

    SHERPA/KODIAK CUB MOBILITY SYSTEM (MANUAL WHEELCHAIR)

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    SPECTRUM MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·April 30, 2013

    EON

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·August 28, 2014

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·May 17, 2011

    FT4, FREE THYROXINE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEC·September 30, 2016