BEUDAMED
    8 results · 21ms · 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.
    Filters Regulation: Us FDA ×

    Senhance Surgical System

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Neuro Cochlear Implant System

    FDA UDI
    NEURELEC·03663227001754·PACKING SET, NEURO2 ZTI EXCHANGE BOX C044

    PHARMAJET STRATIS 0.5 ML NEEDLE-FREE INJECTION SYSTEM MODEL 501-01, STRATIS INJECTOR CATALOG 501-10, STRATIS RESET STATI

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SEDECAL MOBILE DIGITAL DIAGNOSTIC X-RAY

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD¿ HEPARIN SYRINGE 27G X 1/2IN 1ML

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·October 19, 2017

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·June 17, 2013

    NOVOPEN 3 (INSULIN DELIVERY DEVICE) N/A

    FDA Adverse Event
    Other ·NOVO NORDISK A/S, MEDICAL SYSTEMS·Product code FMF·July 12, 2011

    CLARION

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS LLC·Product code MCM·September 25, 2008