BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    Ultra/Phonic Scanning Gel

    FDA 510(k)
    FDA Class 2 ·Radiology

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A163026150·16mm H x 30mm W x 26mm L x 15 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A163026120·16mm H x 30mm W x 26mm L x 12 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A16302680·16mm H x 30mm W x 26mm L x 8 degrees ALIF

    ELECTRO SENSOR -BODY COMPOSITION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OK METER BLOOD GLUCOSE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    WAVEWRITER ALPHA? 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·May 15, 2026

    BD MICROLANCE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·December 12, 2017

    VIVA XT

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·October 10, 2014

    EMAX 2 MOTOR

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·June 11, 2013

    ISE INDIRECT K+ FOR GEN.2

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEM·July 15, 2011