BEUDAMED
    6 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.

    AMERICAN NASAL SPONGE

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    MULTI-IMAGE CAMERA-#627 TLC

    FDA 510(k)
    FDA Class 2 ·Radiology

    3TEST SUPREME GLUCOSE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR - VASCULAR SOLUTIONS·Product code MGB·October 14, 2010

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code ITI·December 13, 2012

    GLUMA DESENSITIZER POWER GEL

    FDA Adverse Event
    Malfunction ·HERAEUS KULZER GMBH·Product code LBH·June 13, 2014