BEUDAMED
    6 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.
    Filters Regulation: Us FDA ×

    OVUM PICK-UP ASPIRATION NEEDLES

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    #400 BROOK AIRWAY & #900 PROFESSIONAL BROOK AIRWAY

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    Lung Vision System

    FDA 510(k)
    FDA Class 2 ·Radiology

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·February 28, 2013

    UNKNOWN DEPUY 36MM METAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·January 31, 2011

    V200 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC.·Product code CBK·July 9, 2014