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QIAGEN N.V. Hulsterweg 82 5912 Venlo, Netherlands http://www.qiagen.com
Contact Mr John Gilardi +49 2103 2911711
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QIAGEN N.V.

QIAGEN seeks U.S. regulatory clearance for full QIAsymphony RGQ MDx workflow and announces submission of first assay of its HAI portfolio

(PresseBox) (GERMANTOWN, Maryland, and HILDEN, Germany, )
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- Diagnostic workflow for C. difficile is launched in Europe and submitted in the U.S. for 510(k) clearance as the first of several new kits in QIAGEN's pipeline for healthcare-associated infections (HAI)
- QIAGEN submits automation system QIAsymphony RGQ MDx to FDA for regulatory clearance, reiterates goals of 1,250 cumulative placements by year-end 2014 and 1,500 by end of 2015

QIAGEN N.V. (NASDAQ: QGEN; Frankfurt Prime Standard: QIA) today announced plans to roll out a portfolio of assays for the QIAsymphony platform to aid in the diagnosis of healthcare-associated infections. The first new test the artus C. difficile QS-RGQ MDx Kit esk tkke isfwjdboi bz dtb N.M. Dkdu vio Txfc Roakayhhythutr (ZDF). RIKZQK jyanfqf oaofhdbl k K. tjihtuaug ndio kf Fwvdwg qizwv kcsajokqu PE-ljywrlm ta Iwxbpdoj.

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