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

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    VITEK 2 ESBL TEST

    FDA 510(k)
    FDA Class 2 ·Microbiology

    VITEK® 2 AST-N350

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·December 17, 2018

    VITEK® 2 AST-N350

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·December 17, 2018

    CD HORIZON® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074037356·BONE SCREW 7040845 ILIAC 8.5X45 TI

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR20408451·Arch wires Titanol Superelastic Straight-Arch-F...

    MODIFICATION TO OSTEONICS SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO JMS A.V. FISTULA NEEDLE SET

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 8, 2013

    RESONANCE STENT SET

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FAD·March 23, 2011

    CIDEX PLUS 28 DAY SOLUTION

    FDA Adverse Event
    Malfunction ·JOHNSON & JOHNSON·Product code LRJ·May 9, 2008

    ULTRACISION HARMONIC ACE (EXACT CODE UNKNOWN)

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·December 17, 2019