BEUDAMED
    6 results · 25ms · 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.

    CEEGRAPH TRAVELER AMBULATORY EEG RECORDER

    FDA 510(k)
    FDA Class 2 ·Neurology

    CONDOR DIGITAL INFLATION SYRINGE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPECTACLE FRAMES+ SUNGLASSSES(NON PRESC.)

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·February 11, 2013

    DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011

    PROSTAR XL SUTURE-MEDIATED CLOSURE

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·July 24, 2014