BEUDAMED
    6 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.

    INTERCEPT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Dorsal Appliance

    FDA 510(k)
    FDA Class 2 ·Dental

    FEATHERLIFT EXTENDED APTOS THREAD

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

    EX-PRESS MINI GLAUCOMA SHUNT

    FDA Adverse Event
    Malfunction ·OPTONOL, LTD·Product code KYF·March 25, 2014

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·October 24, 2012

    OPERON

    FDA Adverse Event
    BERCHTOLD CORP·Product code FWY·September 23, 2010