BEUDAMED
    7 results · 32ms · 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 ×

    DISP. TRANSDUCER W/MONITORING KIT TRANS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GN Otometrics A/S

    FDA UDI
    NATUS MANUFACTURING LIMITED·05713315001727·Silicone Eartip, 9.5 mm semi blue, mushroom

    AIRWAY SUPPORT SYSTEM / AIRPORT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ACCESS IMMUNOASSAY SYSTEM TOXO IGM II ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    OT PING ENHANCED METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 25, 2014

    ENDEAVOR SPRINT RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·November 14, 2012

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code LWS·June 10, 2015