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

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    Momentum™ Posterior Spinal Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994455741·CASE 6191932 ATL TRANS IMP OUTER CASE

    Oticon

    FDA UDI
    Oticon A/S·05707131339850·SIYA 1, KIT 13 NFM R C001

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111452048·RAMSAY FORCEPS SERRATED 2X3 7 INCHES

    HEM-7200-Z (BP742)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IGLUCOSE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·August 4, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 27, 2013

    VAPR S90 ELECTRODE

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code GEI·October 1, 2008