BEUDAMED
    6 results · 19ms · 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 ×

    AMO PROFINESSE III ULTRASONIC HANDPIECE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SI-TECHNOLOGY® SI-DESIS® SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO: CERCON BASE

    FDA 510(k)
    FDA Class 2 ·Dental

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code DXY·February 9, 2013

    COULTER LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·July 22, 2014

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 6, 2011