AB SCIEX displayed the brand new 3200MD Series analyzer at its booth during AACC 2013 this week in Houston, Texas. The analyzer is approved for general in vitro diagnostic use in Europe and is the first of a family of in vitro diagnostic devices that AB SCIEX plans to roll out around the world in the future.
AB SCIEX Displays Diagnostic LC/MS/MS Technology at AACC 2013
Meeting regulatory requirements to obtain the CE-IVDD mark for the new AB SCIEX API 3200MD™and 3200MD QTRAP® LC/MS/MS systems* will provide European hospitals and clinical diagnostic laboratories the confidence to use these mass spectrometry-based systems to improve the quality of results in clinical analysis while reducing costs.
"We are focused on meeting the medical, technological and compliance needs of clinical diagnostic laboratories and hospitals," said Rainer Blair, President of AB SCIEX. "The use of LC/MS/MS technology for clinical diagnostics has already been proven to deliver faster, more accurate results at lower cost compared to existing technologies. Now, we are bringing these benefits to Europe in a way that will simplify and accelerate adoption of this powerful technology."
AB SCIEX plans to roll out regulatory-compliant systems around the world in the future. With these IVD devices, the company is delivering on its strategy to expand the use of its technology in clinical diagnostics, which is widely deemed a new frontier for mass spectrometry.
AB SCIEX has a two-decade track record of success in the clinical research (RUO) market. The company has excelled at advancing and simplifying LC/MS/MS technology, so it is easier for laboratories to adopt and utilize for routine analysis. The robustness and ease of use of the 3200 product line makes it a preferred instrument for research laboratories of all sizes. Now applying its expertise and experience to the IVD market, AB SCIEX is also expanding its service offerings to provide enhanced service and support specifically for clinical diagnostics.
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