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

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    PAPER POINTS

    FDA 510(k)
    FDA Class 1 ·Dental

    Lancer Gear

    FDA UDI
    LANCER ORTHODONTICS, INC.·00817573023837·CERVICAL"LANCER GEAR"BLACK/LIGHT BLUE 5/PACK

    Denture Base Resin

    FDA 510(k)
    FDA Class 2 ·Dental

    DISCOVERY MR750W 3.0T

    FDA 510(k)
    FDA Class 2 ·Radiology

    C-SERIES PORTABLE SCALE ASSEMBLY

    FDA Adverse Event
    Malfunction ·PRISM MEDICAL·Product code FSA·May 8, 2014

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·November 13, 2012

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·September 10, 2010

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP.·Product code NIQ·October 3, 2007