BEUDAMED
    54 results · 26ms · Sources: EU EUDAMED, US FDA

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    MLS-AC DERMA SCANNER

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741014300·

    BI-CONCAVE LENS

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111611·

    Needle Guide

    FDA UDI
    CIVCO MEDICAL INSTRUMENTS CO., INC.·10841436118276·Sterile endocavity needle guide with (2x20cm) a...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L101430120·10mm H x 14mm W x 30mm L XLIF Trial 12 degree L...

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674101430060·

    RESPIRTECH PRO-O2C, MODEL 2200 AND RESPIRTECH PRO, MODEL 2000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ACTIWARE-PLMS

    FDA 510(k)
    FDA Class 2 ·Neurology

    LOFRIC PRIMO

    FDA Adverse Event
    Malfunction ·WELLSPECT HEALTHCARE·Product code EZD·March 20, 2026

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·October 17, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·December 28, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·October 12, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·August 9, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·July 18, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·July 18, 2017

    VASO VIEW HEMOPRO

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·May 3, 2013

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 3, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·May 24, 2011

    CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·August 14, 2017

    EVOLUTION BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FAD·March 12, 2015