BEUDAMED
    10,000 results · 74ms · 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 ×

    U OF I STERNUM NEEDLE 15GA

    FDA Adverse Event
    Injury ·ALLEGIANCE HEALTHCARE CORPORATION·Product code FMI·August 18, 2000

    EASYTOUCH

    FDA Adverse Event
    Malfunction ·BERPU MEDICAL TECHNOLOGY CO., LTD·Product code FMF·May 28, 2026

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·February 6, 2011

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON-IRVINE TECHNOLOGY CTR.·Product code HQE·November 3, 2005

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·January 6, 2011

    MAXPLUS TRI-FUSE EXTENSION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP.·Product code FPA·November 20, 2013

    GC 10F 80CM VISTA BRITE

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DQY·February 4, 2010

    ENDO GIA II 60-4.8 SULU

    FDA Adverse Event
    Injury ·USSC PUERTO RICO·Product code GDW·July 13, 2011

    BD ALARIS SMARTSITE EXTENSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·March 24, 2022

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM INC.·Product code MDS·February 18, 2014

    STYLE 410 COHESIVE SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·June 6, 2023

    BD IV SET SN404 W/O BP Y-CONN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FOZ·February 20, 2018

    HICKMAN

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code LJT·October 14, 1998

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code FPA·June 29, 2012

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code FPA·June 29, 2012

    TUBING, PUMP, CARDIOPULMONARY BYPASS22

    FDA Adverse Event
    Malfunction ·LIVANOVA USA INC·Product code DWF·October 11, 2019

    IV SET BN310 W/O BP Y-CONN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FOZ·June 12, 2019

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON LABORATORIES INC.·Product code HQE·April 9, 1998

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQE·April 9, 1998

    MEDI-TECH

    FDA Adverse Event
    Injury ·MEDI TECH·Product code FOZ·October 23, 2002