BEUDAMED
    10 results · 22ms · 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.
    Filters Regulation: Us FDA ×

    Alphenix, INFX-8000V/B, V8.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L181670120·18mm H x 16mm W x 70mm L XLIF Trial 12 degree L...

    UNITED U2 BIPOLAR IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    THE ADVANTAGE SERIES NON-VENTED (NV) FULL FACE MASK

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    S-ROM M HEAD 36MM +0

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 21, 2013

    FLEXCATH STEERABLE SHEATH

    FDA Adverse Event
    Malfunction ·MEDTRONIC CRYOCATH LP·Product code DRA·July 27, 2011

    MAVERICK2 MONORAIL PTCA CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LOX·September 30, 2008

    INTRAUTERINE ACCESS BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LKF·December 10, 2020

    INVICTUS SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·ALPHATEC SPINE, INC.·Product code NKB·April 30, 2025

    SELECTIVE SALPINGOGRAPHY CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LKF·November 19, 2021