BEUDAMED
    11 results · 28ms · Sources: EU EUDAMED, US FDA

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    DRX-Revolution Nano Mobile X-ray System

    FDA 510(k)
    FDA Class 2 ·Radiology

    ENDOLUMINAL OCCLUSION SYSTEM (EOS)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEPUY GRIPTION TF 5.5MM STERILE LOCKING SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OPTICROSS? HD

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·July 1, 2025

    BD VACUTAINER® ECLIPSE¿ SIGNAL¿ BLOOD COLLECTION NEEDLE WITH INTEGRATED HOLDER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 8, 2018

    BD VACUTAINER® ECLIPSE¿ SIGNAL¿ BLOOD COLLECTION NEEDLE WITH INTEGRATED HOLDER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 18, 2018

    TBD

    FDA Adverse Event
    Malfunction ·Product code KOD·April 5, 2018

    EVIA DR-T

    FDA Adverse Event
    Death ·BIOTRONIK SE & CO. KG·Product code DXY·June 17, 2013

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·July 24, 2011

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·October 1, 2014

    BD SOLOMED¿ SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMF·January 11, 2019