BEUDAMED
    7 results · 27ms · 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.

    PATHFINDER DIRECT ANTIGEN DETECTION SYS ROTAVIRUS

    FDA 510(k)
    FDA Class 1 ·Microbiology

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·10842209120977·

    Genesis Low Temperature Reusable Rigid Container System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    COMPUFLO

    FDA 510(k)
    FDA Class 2 ·General Hospital

    FLEXI-SEAL CONTROL FMS KIT US

    FDA Adverse Event
    Malfunction ·CONVATEC INC.·Product code KNT·April 3, 2014

    VITALITY

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 5, 2010

    FIBREKOR POST

    FDA Adverse Event
    Injury ·PENTRON CLINICAL·Product code ELR·December 3, 2012