BEUDAMED
    24 results · 27ms · 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 ×

    ID NOW COVID-19 2.0 TEST KIT 24T (EUA)

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·February 7, 2023

    ID NOW COVID-19 2.0 TEST KIT 24T (EUA)

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·February 22, 2023

    ASSEMBLY NAC-Y SITE (0.088 TUBING) OEM

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·July 23, 2020

    BD ASSEMBLY NAC-Y SITE

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS S.A. DE C.V.·Product code FPA·December 12, 2023

    ASSEMBLY NAC-Y SITE (0.088 TUBING)

    FDA Adverse Event
    Malfunction ·Product code FPA·September 14, 2021

    BD ASSEMBLY NAC-Y SITE (0.088 TUBING) OEM

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS S.A. DE C.V.·Product code FPA·February 10, 2025

    ASSEMBLY NAC-Y SITE (0.088 TUBING) OEM

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·February 12, 2021

    ASSEMBLY NAC-Y SITE (0.088 TUBING) OEM

    FDA Adverse Event
    Malfunction ·Product code FPA·August 16, 2021

    UNSPECIFIED BD Y-SITE BLUE VALVE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·June 30, 2020

    BD ALARIS¿ ASSEMBLY NAC Y-SITE TUBING

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·July 8, 2022

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 26, 2013

    DRIVE SHAFT-MINIMUM 360MM LENGTH-FOR USE WITH RIA

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HTO·September 18, 2014

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 13, 2011

    THV 1000-27 3F AORTIC BIO 27MM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·October 12, 2020

    THV 1000-27 3F AORTIC BIO 27MM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·October 20, 2020

    THV 1000-27 3F AORTIC BIO 27MM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVE DIVISION·Product code LWR·June 14, 2019

    THV 1000-27 3F AORTIC BIO 27MM

    FDA Adverse Event
    Injury ·MEDTRONIC ATS 3F THERAPEUTICS·Product code LWR·November 9, 2012

    THV 1000-27 3F AORTIC BIO 27MM

    FDA Adverse Event
    Injury ·MEDTRONIC ATS 3F THERAPEUTICS·Product code LWR·December 7, 2012

    THV 1000-27 3F AORTIC BIO 27MM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·March 13, 2019

    THV 1000-27 3F AORTIC BIO 27MM

    FDA Adverse Event
    Injury ·MEDTRONIC 3F THERAPEUTICS, INC.·Product code LWR·December 2, 2024