BEUDAMED
    9 results · 20ms · 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 ×

    MARDX LLYME DISEASE EIA (IGG & IGM) TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123281·K-WIRE - DOUBLE TROCAR 2.0mm DIA x 150mm

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756244084·GENERAL MAJOR TRAY

    V. Mueller

    FDA UDI
    CAREFUSION 2200, INC·10885403155758·DIAMOND-TOUCH® NEEDLE HOLDER, MAYFIELD MICRO R...

    32mm Glenosphere and Humeral Cup

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDTRONIC BURR HOLE PLUG & CAP

    FDA 510(k)

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 10, 2014

    NATURAL-KNEE II CONGRUENT TIBIAL INSERT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·October 26, 2010

    DST SERIES EEA ORVIL 25MM DEVICE

    FDA Adverse Event
    Injury ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GAG·December 21, 2012