BEUDAMED
    8 results · 19ms · 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.

    ISO-DATA 500 SERIES GAMMA COUNTER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867314146·Low Profile Screw, 2.4 x 30mm, Cortical

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867045279·LOW PROFILE SCREW, 2.4 X 30MM, CORTEX

    ZOLL PEDIPADZ REDUCED ENERGY ELECTRODE

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    ArgenIS Titanium Abutments

    FDA 510(k)
    FDA Class 2 ·Dental

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 2, 2014

    RESTORE ADVANCED RECHARGEABLE

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·October 11, 2010

    UNKNOWN MIS BUR

    FDA Adverse Event
    Malfunction ·STRYKER IRELAND LTD.·Product code HBE·December 11, 2012