BEUDAMED
    7 results · 18ms · 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.

    A COMPANY BRASS SEPARATING RINGS

    FDA 510(k)
    FDA Class 1 ·Dental

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209106615·KIT, GUN SHOT WOUND FIRST AID - RED

    Video Colposcope

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

    MODEL B BIPOLAR ENDOCARDIAL LEAD

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    2008K 2 HEMODIALYSIS MACHINE

    FDA Adverse Event
    Malfunction ·CONCORD MANUFACTURING·Product code KDI·April 17, 2014

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·October 4, 2010

    COULTER® LH 500 INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code GKZ·November 29, 2012