BEUDAMED
    10 results · 28ms · 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 ×

    TRUMPF MEDICAL

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code GDC·December 22, 2025

    BD INTIMA-II Y 18GAX1.16IN PRN EC SLM NPVC

    FDA Adverse Event
    Malfunction ·BD SUZHOU (MDS)·Product code FOZ·April 8, 2024

    VENTILATION TUBE 7080100 HUNSAKER MON-JE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code BTR·February 24, 2012

    VENTILATION TUBE 7080100 HUNSAKER MON-JE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code BTR·February 24, 2012

    VENTILATION TUBE 7080100 HUNSAKER MON-JE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code BTR·February 24, 2012

    BD INTIMA¿-II Y CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·August 15, 2023

    DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·April 26, 2013

    INTELLIVUE MULTI MEASUREMENT SERVER X2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·April 6, 2011

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER CORP, MEDICAL DIVISION·Product code FNL·July 17, 2008

    JET VENTILATION - HUNSAKER MON-JET VENTILATION TUBE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code BTR·December 5, 2016