BEUDAMED
    11 results · 22ms · 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.

    ClotTriever Thrombectomy System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HeartLight

    FDA UDI
    CARDIOFOCUS, INC.·00868976000109·Laser Ablation Balloon Catheter

    MUCOGRAFT

    FDA 510(k)
    FDA Class 2 ·Dental

    VITREA CT MYOCARDIAL ANALYSIS

    FDA 510(k)
    FDA Class 2 ·Radiology

    VENTRICULAR PRESSIO CATHETER

    FDA Adverse Event
    Injury ·SOPHYSA·Product code GWM·August 23, 2018

    LIGAMAX-5MM ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 21, 2013

    HUDSON INCENTIVE SPIROMETER LUNG VOLUME EXERC.

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BWF·July 8, 2011

    ABBOTT M2000SP

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code JJH·October 17, 2014

    MEDOS PROG INFANT VALVESYSTEM

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES MANSFIELD·Product code JXG·January 12, 2023

    URETERAL BRUSH BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FDX·November 15, 2023

    URETERAL BRUSH BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FDX·January 7, 2022