BEUDAMED
    153 results · 60ms · 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 ×

    MOBETRON

    FDA UDI
    INTRAOP MEDICAL CORPORATION·00861396000308·The MOBETRON is intended for use as an Electron...

    Mobetron Model 1000, mobile electron linear accelerator, a device system which delivers radiation to an intraoperative site.

    FDA Recall
    Terminated ·Intraop Medical Corporation·Product code LHN·June 20, 2008

    SPYGLASS DISCOVER DIGITAL CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FBN·June 24, 2024

    CRS® ROTARY MIXER CEMENT 5CC STERILE

    FDA Adverse Event
    Death ·SYNTHES MONUMENT·Product code GXP·January 24, 2014

    DETACHABLE POUCH 3X6

    FDA Adverse Event
    Malfunction ·UNIMAX MEDICAL SYSTEMS INC·Product code GCJ·July 21, 2017

    ANS QUATTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Other ·ADVANCED NEUROMODULATION SYSTEMS, INC·Product code LGW·August 6, 2007

    ANS QUATTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Other ·ADVANCED NEUROMODULATION SYSTEMS, INC·Product code LGW·August 6, 2007

    MEDTRONIC NAVIGATION

    FDA Adverse Event
    Injury ·MEDTRONIC NAVIGATION, INC.·Product code HAW·January 27, 2026

    TERUMO RADIFOCUS GUIDE WIRE

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

    R2P MISAGO

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code NIP·July 2, 2025

    URINARY TRACT OCCLUSION BALLOON CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KOD·February 18, 2024

    HEMASHIELD PLATINUM WOVEN DOUBLE VELOUR

    FDA Adverse Event
    Injury ·INTERVASCULAR SAS·Product code MAL·October 2, 2018

    LUER ADAPTER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION - KOFU·Product code JKA·June 20, 2022

    RUNTHROUGH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·September 16, 2025

    GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 1, 2025

    ANGIO-SEAL

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code MGB·February 17, 2026

    EVIS LUCERA GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·June 2, 2022

    EVIS LUCERA ELITE GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·June 2, 2022

    ROTATABLE CLIP FIXING DEVICE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code MND·June 2, 2022

    DISPOSABLE ELECTROSURGICAL SNARE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDI·June 2, 2022