BEUDAMED
    116 results · 20ms · 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.

    AT-2

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    PROFYLE

    FDA UDI
    Stryker GmbH·34546540244834·BONE SCREWS, CROSS-FIT, SELF-TAPPING

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111031·INSTRUMENT CADDY LARGE

    Forcep

    FDA UDI
    KOROS U.S.A., INC.·10840199539489·Mixter Forceps 18cm 7"

    DISTAL RADIUS FRACTURE REPAIR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VERI-Q MGD-1001 BLOOD GLUCOSE MONITORING SYSTEM, VERI-Q PLUS MGD-1001 BLOOD GLUCOSE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    RADIFOCUS GLIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 22, 2018

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·December 13, 2010

    DIMENSION XPAND PLUS WITH HM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·July 9, 2014

    AFFINITY THREE BIRTHING BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code HDD·December 27, 2012

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·December 29, 2025

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO MEDICAL CORPORATION·Product code DQX·May 16, 2024

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 21, 2021

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·October 6, 2025

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO MEDICAL CORPORATION·Product code DQX·September 15, 2023

    GUIDE WIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 25, 2025

    RADIFOCUS GUIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO MEDICAL CORPORATION·Product code DQX·December 5, 2023

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 3, 2018

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 23, 2026

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 11, 2026