They played a vital role in leading the implementation of CTLM
practices, strategies and philosophies in their schools.
IDSI will select new distributors for the UAE and intends to secure prospective sales of the CTLM
system based on leads from the RSNA 2008 conference.
Selling a CTLM
system in this important emerging market will only further accelerate our goal of it becoming a commonly used method for breast imaging throughout this area.
Their work demonstrated an increase in accuracy of diagnosing malignant and benign breast lesions in patients who were examined with mammography and CTLM
adjunctively compared to mammography alone.
This agreement requires ID-Matrix to order a minimum of 15 CTLM
systems within the first year of the contract along with a 50% deposit with each order to remain as the company's exclusive distributor.
Her study, which evaluated CTLM
as an adjunct to mammography in women with heterogeneously or extremely dense breast tissue, found that CTLM
could successfully distinguish malignant from benign lesions in dense breasts.
PreMarket Approval from the Food and Drug Administration for its CTLM
system to be used as an adjunct to mammography.
Andras Vertes, CEO/MDHC commented, "I am looking forward to working with the CTLM
system and believe it will fit in very well with our other modalities.
Fluorescence Markers" is a compound that the company is currently studying in conjunction with major pharmaceutical companies as an advanced diagnostic feature to be used with the company's laser mammography system: The CTLM
in combination with the fluorescent feature has the potential to be used with photodynamic therapy to aid in the treatment of breast cancer.
system will be placed in the prestigious hospital Hadassah, located in the heart of Jerusalem.
IDSI) (OTCBB:IMDS) a pioneer in optical breast imaging announced that it has received notification from the Food and Drug Administration (FDA) that the review of the company's Section 510(k) pre-market notification application of its CTLM
system has been completed and categorized as a Class III device requiring a Premarket Approval application.
system has received certification and licenses to sell internationally European CE marking, CMDCAS Canadian License, China SFDA, UL, ISO 9001:2000, ISO 13485:2003 and FDA export certification.