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Dilon erhält CE-Zulassung für sein Navigator-Gamma-Sondensystem
Date:7/10/2014

NEWPORT NEWS, Virginia, 11. Juli 2014 /PRNewswire/ -- Dilon Technologies, ein führender Hersteller von Kameras für die molekulare Bildgebung, einschließlich molekularer Bildgebung der Brust (MBI/BSGI), hat heute die CE-Zulassung für sein Navigator®-Gamma-Sondensystem bekanntgegeben. Mit dem CE-Zeichen kann Dilon das Produkt jetzt europaweit vertreiben. Dilon hat seinen Vertriebsbereich auf den Großteil der europäischen Länder ausgedehnt und bereits die ersten Bestellungen erhalten.

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„Die Navigator-Gamma-Sonde wurde von Chirurgen in den USA auf breiter Basis angenommen. Drei Hauptgründe für die Akzeptanz unter Chirurgen waren die große Zuverlässigkeit, das einfache Design und die unkomplizierte Handhabung", sagte Robert Moussa, President und CEO von Dilon. „Für Europa und andere Länder weltweit, die das CE-Zeichen anerkennen, erwarten wir eine ähnliche Marktreaktion."

Das Navigator-Gamma-Sondensystem wird bei radionuklidgestützten chirurgischen Eingriffen verwendet, hauptsächlich beim Lymphknoten-Mapping und bei der Lokalisation von Tumoren. In den vergangenen Jahrzehnten haben sich Verfahren wie das Wächterlymphknoten-Mapping, zunächst bei Melanomen und jüngst bei der Brust, bei Allgemeinchirurgen und chirurgischen Onkologen zum Goldstandard bei der Behandlung entwickelt. Weitere Einsatzgebiete der Navigator-Gamma-Sonde sind die thorakoskopische Wedge-Resektion, Adenome der Nebenschilddrüse und Laparoskopie.

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Dilon Technologies® Inc. entwickelt innovative Medizinprodukte, die die Lebensquali
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