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Digital System Receives European Mammographic Certification

By MedImaging International staff writers
Posted on 14 Apr 2011
A European Certification for a digital mammography system ensures users that the digital mammography system meets or exceeds rigorous European image quality and dose standards.

Hologic, Inc. (Bedford, MA, USA), a developer, manufacturer, and supplier of diagnostics products, medical imaging systems, and surgical products dedicated to serving the healthcare needs of women, reported that its Selenia Dimensions digital mammography system in two-dimensional (2D) mode has been awarded EUREF type test certification by the European Reference Organization Council for Quality Assured Breast Screening and Diagnostic Services (EUREF; Nijmegen, The Netherlands). Only three products have received EUREF approval to date, of which two are Hologic systems--namely, the Selenia digital mammography system and now Selenia Dimensions, a breast cancer screening and diagnosis technology.

The mission of the nonprofit EUREF council is to raise standards by bringing together, at the European level, the best examples of quality control in mammography screening from regional and national breast cancer screening programs. EUREF mammographic type test certification ensures hospitals and imaging centers that the Hologic Selenia Dimensions system in 2D mode has passed a rigorous series of physics and clinical tests demonstrating the system meets the image quality, radiation exposure, and stability standards set by EUREF for screening and diagnostic mammography equipment.

"Hologic has a reputation for following rigorous manufacturing standards and processes including International Organization for Standardization registration and CE mark certification for our Selenia and Selenia Dimensions digital mammography systems,” said David Harding, senior vice president and general manager, International at Hologic. For some time we have been offering our Selenia Dimensions system in 2D and/or 3D mode in our international markets. On February 11, 2011, the US Food and Drug Administration [FDA] approved using the Selenia Dimensions system in either or both modes in the US. The quality and stability of the system certified by EUREF combined with the recent 3D approval by the FDA sets the Selenia Dimensions breast cancer screening and diagnostic platform in a class of its own.”

Related Links:
Hologic
European Reference Organization


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