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Address: 6392 Via Real, Carpinteria, California 93013, USA
www.dakousa.com |
Send Inquiry |
Phone: +1-(805)-566-6655, 800-235-5743
FDA Registration: 2022180 Annual Revenues: USD 25-50 Million
Employee Count: ~180
Quality: ISO 9001 Certified
Products: Albumin Antigen Antiserum Control (FDA Code:
DCF), Albumin, FITC Conjugate (FDA Code:
DDZ), 2 Herpesvirus Hominis 1 Cf Antisera (FDA Code:
GQO), 2 Herpesvirus Hominis 1 Fluorescent Antisera (FDA Code:
GQL), Acid Fuchsin Stain (FDA Code:
IDF), Alcian Blue Stain (FDA Code:
IDA), ...
Dako North America, Inc. focuses on tissue-based cancer diagnostics like immunohistochemistry, in situ hybridization, flow cytometry, bulk antibodies for turbidometry and ELISA kits. We provide reagen
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Address: 4300 N. Harbor Boulevard P.O. Box 3100, Fullerton, California 92834-3100, USA
www.coulter.com |
Phone: +001-(800)-742-2345
FDA Registration: 2050012 Year Established: 1934
Annual Revenues: > USD 1 Billion
Employee Count: ~10100
Quality: ISO 9000, ISO 9001, ISO 9002, CE Certified
Products: Hematology Analyzers, Blood Analyzer Reagents, Chemistry Analyzers, Controls for Diagnostic Equipment, Hematology Reagents, General Diagnostic Supplies, ...
Beckman Coulter, Inc. is a manufacturer of biomedical testing instrument systems, tests & supplies that simplify and automate laboratory processes. Spanning the biomedical testing continuum from medic
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Address: 378 Page St., Stoughton, Massachusetts 02072-1141, USA
www.btiinc.com |
Phone: +1-(781)-344-9942
Year Established: 1981
Annual Revenues: USD 1-5 Million
Employee Count: ~10
Products: Disposable Pipette Tips, Non-sterile Disposable Tips, Bone Wax (FDA Code:
MTJ), Cyclic AMP Radioimmunoassay Test (FDA Code:
CHO), Cyclic GMP Radioimmunoassay Test (FDA Code:
CGT), Diagnostics Contract Research & Development, Calcium Compound Bone Void Filler (FDA Code:
MQV), ...
Biomedical Technologies, Inc. manufactures growth factor and attachment factor products. Our extensive product line includes receptor-grade, aseptically packaged GFs and AFs. These are highly purified
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FDA Code / Regulation: JMR / 862.1490 A lysozyme (muramidase) test system is a device intended to measure the activity of the bacteriolytic enzyme lysozyme (muramidase) in serum, plasma, leukocytes, and urine. Lysozyme measurements are used in the diagnosis and treatment of monocytic leukemia and kidney disease.
Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in 862.9.