BEUDAMED
    10 results · 20ms · 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 Regulation: Us FDA ×

    XOMED TREACE JET VENTILATION TUBE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    GUIDANT PROXIMAL SEAL SYSTEM, MODELS PSS-4500 & PS-4500

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Endolumik Fluorescence Guided Gastric Calibration Tube (FG Bougie)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    HEARTMATE 3 VAD MODULAR CABLE

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·June 12, 2025

    BASIX COMPAK INFLATION SYRINGE KIT

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code DXT·December 15, 2011

    BASIX COMPAK INFLATION SYRINGE KIT

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code MAV·December 15, 2011

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 13, 2010

    DIMENSION VISTA 500

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·January 18, 2013

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 9, 2014

    HEARTMATE 3 VAD MODULAR CABLE

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·June 12, 2025