Teco is the industry leader in the manufacturing of vitro clinical diagnostic tests and instruments, from urinalysis to ELISA. Located in Anaheim, CA the manufacturing is FDA regulated and all production is under based on Current Good Manufacturing Practices (cGMP) regulations. Teco’s ISO 13485 certification verifies that the company meets the international standard for medical device Quality Management Systems.
Product testing modules are available for urinalysis, clinical chemistry, hematology, serology, immunochemistry and electrolytes. Teco offers point-of-care rapid testing for; cardiac markers, h. pylori, malaria, dengue fever, Chlamydia, syphilis, as well as, tests for drug adulteration and alcohol.
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