BEUDAMED
    8 results · 26ms · 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.

    X-RAY TUBE, ROTATING ANODE

    FDA 510(k)
    FDA Class 1 ·Radiology

    Nautilus Delta E Adaptor

    FDA UDI
    Bard Access Systems, Inc.·00801741144615·Nautilus Delta TCS Electrical Adaptor

    STOCKERT NEURO N50, MODEL12267

    FDA 510(k)
    FDA Class 2 ·Neurology

    BD Nexiva Closed IV Catheter System (Single Port) with MaxZero Needleless Connector

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LEAD MODEL 304

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·April 24, 2014

    ONE TOUCH PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·May 14, 2010

    HEARTMATE II LEFT VENTRICULAR ASSIST DEVICE

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·October 1, 2012

    Exactech Equinoxe CAGE GLENOID, CEMENTED, alpha curvature, Mates with: a) 38, 41, 44 head, Small, Item Number 314-13-02, b) 38, 41, 44 head, Medium, Item Number 314-13-03, c) 38, 41, 44 head, Large, Item Number 314-13-04; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024