BEUDAMED
    352 results · 38ms · Sources: EU EUDAMED, US FDA

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    CT COMPATIBLE F/S/D APPLICATORS

    FDA 510(k)
    FDA Class 2 ·Radiology

    SHIELDING NEEDLE HOLDER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ADVANCED LUNG ANALYSIS-1

    FDA 510(k)
    FDA Class 2 ·Radiology

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·April 11, 2013

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·April 19, 2011

    DELTEC COZMO INSULIN PUMP

    FDA Adverse Event
    Injury ·SMITHS MEDICAL MD (FORMERLY DELTEC, INC)·Product code LZG·June 19, 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

    4.0MM TI QUICK LOCK CANCELLOUSSCREW SELF-DRILLING 18MM

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·March 13, 2015

    TI CERVICAL SPINE LOCKING PL VARIABLE ANGLE 3 LEVEL/48MM

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code KWQ·March 13, 2015

    4.0MM TI QUICK LOCK CANCELLOUS SCREW SELF-DRILLING 20MM

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·March 13, 2015

    SELF-RETAINING SCREWDRIVER FOR QUICK LOCK SCREWS

    FDA Adverse Event
    Injury ·SYNTHES HAGENDORF·Product code HXX·March 13, 2015

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 20, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 9, 2025

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 9, 2025