BEUDAMED
    60 results · 21ms · 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 ×

    VERSALVENT MODEL V1 HYPERBARIC CHAMBER VENTILATOR MODEL V1

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776180072·GENERAL NEEDLE FORCEPS . TC

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169606463·SPACER 2122560 O25 23.5MM 12 DEG 16X60

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780180371·Integra® Jarit® General Needle and Tissue Force...

    RUSCH

    FDA UDI
    TELEFLEX INCORPORATED·24026704624441·RUSCH Color Coded Guedel Airway Length 60mm Tra...

    SCOTT'S SELECT K-FILES 6/pk 25mm # 60

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D77811225601·ENDODONTIC K-FILES (6/pack) Length: 25mm, Size:...

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916120368·ZEUS®-L Hyper, 12 x 25 x 60mm, 14 Degree

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916141561·ZEUS® LLIF 12mm x 25mm x 60mm x 14° TRIAL

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916141523·ZEUS® LLIF 12mm x 25mm x 60mm x 07° TRIAL

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916134549·ZEUS®-L, Lateral Lumber Interbody Fusion Device...

    REPROCESSED PULSE OXIMETER SENSORS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    M2 SINGLE USE MICROKERTOME

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 28, 2018

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·May 21, 2013

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·September 26, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 14, 2011

    RADIFOCUS GLIDEWIRE ADVANTAGE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 1, 2020

    BD CONNECTA¿ STOPCOCK

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·October 7, 2019

    GLIDEWIRE ADVANTAGE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 9, 2025

    RADIFOCUS GLIDEWIRE ADVANTAGE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 23, 2022