EY Laboratories, Inc.

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Web: http://www.eylabs.com
E-Mail:
Address: 107-127 N. Amphlett Blvd., San Mateo, California 94401, USA
Phone: +1-(650)-342-3296, (800)-821-0044 | Fax: +1-(650)-342-2648 | Map/Directions >>
 
 

Profile: Ey Laboratories, Inc. produces rapid, simple & stable diagnostic test kits for visual and qualitative tests. We are an ISO 9001, CE MARK certified company. We offer products such as pure erythrina cristagalli lectin, pure phytolacca americana lectin, crude phytolacca americana lectin, pure urtica dioica lectin & FITC conjugated canavalia ensiformis lectin. Our portable instruments for quantitative assay serve the research, health care and environmental industries. Our Instant Chek System™ combines the latest advances in immunoassay technology, optics, electronics & computing and is possible to obtain quantitative analyte test results in seconds.

The company was founded in 1978, has revenues of USD 1-5 Million, has ~10 employees and is ISO 9001, CE certified.

7 Products/Services (Click for related suppliers)  
• Diagnostic Test Kits
• Gonorrhea Test Kits
• Microorganism Differentiation Strip and Reagent Disc (FDA Code: JTO / 866.2660)
A microorganism differentiation and identification device is a device intended for medical purposes that consists of one or more components, such as differential culture media, biochemical reagents, and paper discs or paper strips impregnated with test reagents, that are usually contained in individual compartments and used to differentiate and identify selected microorganisms. The device aids in the diagnosis of disease.
• Neisseria Gonorrhoeae Identification Kit (FDA Code: JSX / 866.2660)
• Oxidase Test Device for Gonorrhea (FDA Code: LGA / 866.2420)
An oxidase screening test for gonorrhea is an in vitro device that consists of the articles intended to identify by chemical reaction, cytochrome oxidase, an oxidizing enzyme that is associated with certain bacteria includingNeisseria gonorrhoeae. A sample of a male's urethral discharge is obtained on a swab which is placed into a wetting agent containing an ingredient that will react with cytochrome oxidase. When cytochrome oxidase is present, the swab turns a dark purple color within 3 minutes. Because it is unlikely that cytochrome oxidase-positive organisms other thanNeisseria gonorrhoeae are present in the urethral discharge of males, the identification of cytochrome oxidase with this device indicates presumptive infection of the patient with the causative agent of gonorrhea.
• Streptococcal Multiple Exoenzyme Test (FDA Code: GTP / 866.3720)
• Swabs, Gonorrhea Test Kits

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