BEUDAMED
    56 results · 22ms · Sources: EU EUDAMED, US FDA

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    POWDER FREE NITRILE EXAMINATION GLOVES (6MIL), TESTED FOR USE WITH CHEMOTHERAPY DRUGS (BLUE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1016300·10mm H x 16mm W x 30mm L x 0 degrees XLIF

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00860006434564·Tasso+ convenience kit allows self-collection o...

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981265526·Trial, 31mm x 24mm x 16mm, 30 Deg

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981246280·Interbody, 31mm x 24mm x 16mm, 30 Deg

    Sklar®

    FDA UDI
    SKLAR CORPORATION·50649111359796·SKLAR KLEEN POWD 3 1/2 LB CS/6

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X10163080·10mm H x 16mm W x 30mm L x 8 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X101630120·10mm H x 16mm W x 30mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L101630120·10mm H x 16mm W x 30mm L XLIF Trial 12 degree L...

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383502030·Gutta Percha Points is used to root canal filin...

    LEKON

    FDA UDI
    C A I INDUSTRIES CORP·00807689022022·Acupuncture needles

    FacetLink System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575081509·Facet Screw

    KSEA BIPOLAR COAGULATING ELECTRODES

    FDA 510(k)
    FDA Class 2 ·Neurology

    G-FORCE PEEK SUTURE ANCHOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    KENSTONE METAL·Product code ITJ·July 20, 2012

    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