BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    OSHER SURGICAL GONIO/POSTERIOR POLE LENS

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    Barco

    FDA UDI
    Barco NV·05415334050044·MDSC-8527 SSTF M2

    Barco

    FDA UDI
    Barco NV·05415334029286·Surgical color monitor

    DENTHESIVE

    FDA 510(k)
    FDA Class 2 ·Dental

    PHILIPS INTEGRIS H/HM SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·January 25, 2013

    COOK SPECTRUM MINOCYCLINE/RIFAMPIN IMPREGNATED TRIPLE LUMEN CENTRAL VENOUS

    FDA Adverse Event
    Injury ·COOK, INC.·Product code DQO·December 21, 2010

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 15, 2014

    FEMORAL NECK SYSTEM PLATE 1 HOLE - STERILE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·January 16, 2019