BEUDAMED
    6 results · 22ms · 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.

    RUBBER DAM

    FDA 510(k)
    FDA Class 1 ·Dental

    CORNING PARAPROTEIN SCREENING

    FDA 510(k)
    FDA Class 2 ·Immunology

    Sonopet iQ Sterilization Tray

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SM204 M-SERIES W/BIG WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER CORP, MEDICAL DIVISION·Product code FPO·November 1, 2010

    UNIFY CRT-D

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code NIK·January 13, 2014

    ADVANCE MALE SLING SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·December 26, 2012