BEUDAMED
    1,150 results · 38ms · 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 FDA Adverse Event ×

    SENSATION CATHETER

    FDA Adverse Event
    Injury ·GETINGE·Product code DSP·May 7, 2024

    FREESTYLE LIBRE 2

    FDA Adverse Event
    Injury ·ABBOTT DIABETES CARE INC·Product code QLG·August 1, 2023

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLR (PR)·Product code NIQ·July 30, 2003

    OPTIGUIDE

    FDA Adverse Event
    Death ·QLT PHOTOTHERAPEUTICS, INC.·Product code GEX·September 25, 1998

    OPTIGUIDE

    FDA Adverse Event
    Death ·QLT PHOTOTHERAPEUTICS, INC.·Product code GEX·October 13, 1997

    OPTIGUIDE

    FDA Adverse Event
    Death ·QLT PHOTOTHERAPEUTICS, INC.·Product code GEX·October 8, 1997

    LEAD EXTRACTION EVOLUTION MECHANICAL DILATOR SHEATH SET

    FDA Adverse Event
    Injury ·COOK VASCULAR INC.·Product code DRE·October 22, 2013

    INRATIO

    FDA Adverse Event
    Other ·ALRE SAN DIEGO, INC.·Product code GJS·July 29, 2011

    INRATIO

    FDA Adverse Event
    Other ·ALRE SAN DIEGO, INC.·Product code GJS·July 29, 2011

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·April 24, 2020

    ULTRASONIC GASTROVIDEOSCOPE

    FDA Adverse Event
    Injury ·SHIRAKAWA OLYMPUS CO., LTD.·Product code ODG·January 19, 2023

    ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE SYSTEM

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION·Product code NTE·February 26, 2014

    EDWARDS LIFESCIENCES SAPIEN 3 TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·November 18, 2025

    SINGLE USE ASPIRATION NEEDLE NA-U200H

    FDA Adverse Event
    Injury ·OLYMPUS AMERICA, INC·Product code FCG·January 19, 2023

    EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS AMERICA, INC·Product code ODG·January 19, 2023

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC·Product code NJE·July 5, 2016

    BOLT FOR FEMORAL NECK SYSTEM 100MM LENGTH-STERILE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code KTT·December 31, 2019

    5 QT CLR CONTAINER

    FDA Adverse Event
    Other ·THE KENDALL CO.·Product code MMK·October 31, 2000

    LS LF GEMSTAR W CLR

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·March 2, 2009

    MAXPLUS CLR POSITIVE DISPLACEMENT CONN

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·May 13, 2021