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Promega Maxwell 16 IVD System CE Marked to the European Union IVD Directive Delivers Combined Solution for Infectious Disease
Date:3/18/2010

The Promega Maxwell® 16 IVD System is CE marked in accordance with the requirements of Directive 98/79/EC on in vitro diagnostic medical devices.

Madison, WI (PRWEB) March 18, 2010 -- The Promega Maxwell® 16 IVD System is CE marked in accordance with the requirements of Directive 98/79/EC on in vitro diagnostic medical devices. The CE mark applies to the instrument, the Maxwell® 16 Blood DNA Purification System and the Maxwell® 16 Viral Total Nucleic Acid Purification System. The bench top automation system is fully compliant with the IVD Directive and supports European clinical laboratories performing diagnostic tests in molecular pathology, transplant HLA, and Infectious disease.

The Maxwell 16 IVD System works to the specific needs of a clinical lab. Addressing the pressure to deliver quick results, especially in the process to determine organ compatibility or to diagnose infectious disease, Maxwell extracts multiple samples faster than manual methods. Up to 16 samples can be purified simultaneously, without user intervention and with higher yield and greater consistency. The unique design of Maxwell® 16 prevents cross contamination. The Maxwell 16 IVD includes integrated bar code reading to help reduce transcription errors, a UV lamp to assist in sanitization of the unit and its compact enough to operate inside a bio-safety cabinet.

“Enabling technologies like the Maxwell 16 can make a meaningful difference in clinical labs that face the accelerated demands of healthcare,” explains Ashley Anderson M.D., Promega Chief Medical Officer, “Labs have told us repeatedly how quickly and accurately they can deliver life saving information and how easy it is to train new technicians. For some it’s actually advanc
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