BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    TECH DYNE - HP-2000, SKREEN TEST, RMS-200

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110935·STERILIZING CASE NARROW

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122833·K-WIRE - DOUBLE TROCAR 0.8mm DIA x 75mm

    ADVOCATE REDI-CODE+BMB-EA001S BLOOD GLUCOSE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PISCES PLUS (DW286 C)

    FDA 510(k)
    FDA Class 2 ·Dental

    CLOSUREFAST

    FDA Adverse Event
    Malfunction ·VNUS MEDICAL TECHNOLOGIES, INC·Product code GEI·November 14, 2010

    XIENCE PRIME LL EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·July 8, 2014

    FERNO 35X AMBULANCE STRETCHER

    FDA Adverse Event
    Malfunction ·FERNO-WASHINGTON, INC.·Product code FPO·October 26, 2012