BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    REAGENT SYSTEM, PROGESTERONE, ARIA

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    ELEVATE™ Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169430723·SPACER 7770732 ELEVATE X-LOR 32X7MM

    Young Specialties

    FDA UDI
    Young Innovations, Inc.·00843471188651·.022 U/L STD. COMB. WELD SZ#32

    Biomate Dental Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    BCI AUTOCON 3304 DIGITAL PULSE OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PLUM XLD 110V L.A.

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD·Product code FRN·February 18, 2014

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·October 3, 2012

    ACCU-CHEK AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 5, 2007