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.

    DIGITAL FUNDUS CAMERA, MODEL CF-60DSI

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Bone Conductor (BC-2)

    FDA UDI
    Natus Medical Denmark ApS·05713315010101·BC-2 Receiver Spare Part Kit

    SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code MQP·October 30, 2017

    ALLON 2001

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DERMASSIST FLUID RESISTANT SURGICAL MASK WITH WRAPAROUND VISOR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VERTE-STACK SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·SOFAMOR DANEK DEGGENDORF GMBH·Product code MQP·January 21, 2010

    VERTE-STACK SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·SOFAMOR DANEK DEGGENDORF GMBH·Product code ODP·November 20, 2009

    STEALTHSTATION TRIA NAVIGATION SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·April 8, 2013

    ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·March 10, 2011

    VITALITY 2 DR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008