BEUDAMED
    338 results · 23ms · Sources: EU EUDAMED, US FDA

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    3TP SOFTWARE OPTION

    FDA 510(k)
    FDA Class 2 ·Radiology

    COR-KNOT MINI®

    FDA UDI
    LSI Solutions, Inc.·00850200006087·COR-KNOT MINI® COMBO KIT Base Package Type - Ki...

    COR-KNOT MINI®

    FDA UDI
    LSI Solutions, Inc.·00850200006292·COR-KNOT MINI® COMBO KIT

    DRX - Ascend System

    FDA UDI
    CARESTREAM HEALTH, INC.·60889971031358·DRX-ASCEND SYSTEM/QG-40-1-R10-T600

    RIVA Pedicle Screw System

    FDA UDI
    XENIX MEDICAL LLC·00840493419237·PRECONTOUR ROD, 5.5mm x 350mm

    RIVA Pedicle Screw System

    FDA UDI
    XENIX MEDICAL LLC·00840493419329·PRECONTOUR ROD, 6.0mm x 350mm

    PATIENT MATCHED TITANIUM ALLOY TROCHLEA

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STARBAND CRANIAL ORTHOSIS

    FDA 510(k)
    FDA Class 2 ·Neurology

    BD ALARIS SMARTSITE NEEDLE-FREE VALVE

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS S.A. DE C.V.·Product code FPA·June 25, 2025

    TOTALCARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·March 5, 2013

    GENESISXP PULSE GENERATOR, 8-CHANNEL

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·March 23, 2011

    EMBRACE PUMP

    FDA Adverse Event
    Malfunction ·ROSS PRODUCTS DIVISION·Product code LZH·April 18, 2008

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD ALARIS SMARTSITE NEEDLE-FREE VALVE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·August 26, 2025

    BD ALARIS SMARTSITE NEEDLE-FREE VALVE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·August 26, 2025

    BD ALARIS SMARTSITE NEEDLE-FREE VALVE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·August 26, 2025