|
Address: 3050 Spruce St., St. Louis, Missouri 63103, USA
www.sigmaaldrich.com |
Send Inquiry |
Phone: +1-(800)-521-8956
FDA Registration: 1937991 Annual Revenues: USD 50-100 Million
Employee Count: ~8000
Quality: ISO 9000, ISO 9001 Certified
Products: Hematology Analyzers, Tissue Processors, Prostatic Acid Phosphatase, PCR Hoods, Plate Sealing Films, Plate Sealing Foils, ...
Sigma-Aldrich is a life science and high technology company. We are an ISO 9000 & ISO 9001 certified company. We offer products such as vitals, titration, syringes, solid phase microextraction, purifi
more...
|
Address: 10 Electronics Avenue, Danvers, Massachusetts 01923, USA
www.rowleybio.com |
Send Inquiry |
Phone: +1-(978)-739-4883
FDA Registration: 1219125 Annual Revenues: < USD 1 Million
Products: Chemical Supplies, General Medical Supplies, General Diagnostics, General Examination Supplies, Stain Sets & Solutions, Eosin Y Stain (FDA Code:
HYB), ...
Rowley Biochemical Inc. supplies biochemical research facilities, university and clinical laboratories with quality in-vitro stains and reagents. We offer quality dyes, stains & biochemical reagents r
more...
|
Address: 70 Cleveland Ave., Bay Shore, New York 11706, USA
www.polyrnd.com |
Send Inquiry |
Phone: +1-(631)-586-0400, 800-645-5825
FDA Registration: 2429783 Year Established: 1969
Employee Count: ~40
Products: Cytology Test Kits, Medicine Cups, Buffer Solution, Water Based Hematology Stainer, Stainless Steel Medicine Cup, Hematoxylin Stain (FDA Code:
HYJ), ...
Poly Scientific manufactures chemicals, stains and reagents for histology, cytology, microbiology, in-vitro diagnostic testing in hospitals, laboratories, & pharmaceutical companies. Our product categ
more...
FDA Code / Regulation: HZY / 864.1850 Dye and chemical solution stains for medical purposes are mixtures of synthetic or natural dyes or nondye chemicals in solutions used in staining cells and tissues for diagnostic histopathology, cytopathology, or hematology.
Classification. Class I (general controls). These devices are exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in 864.9. These devices are also exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of 820.180, with respect to general requirements concerning records, and 820.198, with respect to complaint files.