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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    BodyGuardian Remote Monitoring System (BGRMS v3.0)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NEXUS® BONESCALPEL® 20MM, BLUNT BLADE + IRRIGATION TUBING KIT

    FDA Adverse Event
    Malfunction ·MISONIX, INC.·Product code LFL·February 12, 2025

    BONESCALPEL® 20MM, BLUNT BLADE

    FDA Adverse Event
    Malfunction ·MISONIX, INC.·Product code LFL·February 12, 2025

    Gynomunal

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

    OPEN RADIOTRANSPARENT INTERSOMATIC IMPLANT (ROI)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD VACUTAINER® MULTIPLE SAMPLE LUER ADAPTER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 6, 2025

    BD VACUTAINER® MULTIPLE SAMPLE LUER ADAPTER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 19, 2025

    TOTAL ASR FEM IMP SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·September 12, 2011

    GORE® ACUSEAL VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DSY·November 11, 2014

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 23, 2013