BEUDAMED
    121 results · 34ms · 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.

    ABSORBENT PAD -- MODIFICATION

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867059481·TRIAL, MEDIUM, PEGGED GLENOID

    TM ARDIS INTERBODY SYSTEM INSERTER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SMALL VOLUME NEBULIZER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    RADIFOCUS GLIDEWIRE M

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

    UNK DEPUY DURALOC CUP

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·December 9, 2010

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 22, 2013

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 9, 2014

    TRIAL, MEDIUM, PEGGED GLENOID

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWT·February 4, 2025

    TRIAL, MEDIUM, PEGGED GLENOID

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWT·July 3, 2023

    TRIAL, MEDIUM, PEGGED GLENOID

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWT·May 3, 2024

    LAPRO-CLIP

    FDA Adverse Event
    Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GCJ·June 4, 2025

    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