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Address: 3130 Gateway Dr, Norcross, Georgia 30091, USA
www.immucor.com |
Phone: +1-(770)-441-2051
FDA Registration: 1034569 Year Established: 1982
Annual Revenues: USD 100-500 Million
Employee Count: ~610
Quality: ISO 9001, CE Certified
Products: Neurology Instruments, Blood Bank Test Kits, Blood Bank Automation, Blood Grouping Reagents, Automated Blood Grouping and Antibody Test System (FDA Code:
KSZ), Frozen Blood Processor (FDA Code:
KSW), ...
Immucor Inc specializes in in-vitro diagnostics. We offer hospital blood banks, clinical laboratories and blood donor centers. We provide automated instruments, traditional reagents and specialty prod
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Address: 9700 Great Seneca Highway Suite 156, Rockville, Maryland 20850, USA
www.hememics.com |
Send Inquiry |
Phone: +1-(301)-560-0415
Products: Imaging Systems for Mammalian Cell Colony Counting, Peptides, Blood Grouping Substance (FDA Code:
KSX), Human and Animal Sera (FDA Code:
KIS), General Purpose Reagent (FDA Code:
LDT), Immunohistochemistry Reagents And Kits (FDA Code:
NJT), ...
Hememics Biotechnology, Inc. manufactures and supplies in-vitro reagents to the health care and pharma industries. The Hemedri™ technology platform is used for preserving & storing of mammalian
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Address: No. 2/1/8, Nelson Manickam Road, F - 4, Karthick Tower, 1st Floor, Choolaimedu, Chennai, Tamil Nadu 600 094, India
www.bloodgroupingreagents.com |
Send Inquiry |
Phone: +91-(44)-42170743
Products: Cotton Crepe Bandage, Diagnostic Reagents, Serology Test Kit, Rapid Plasma Reagent Card Test for Syphilis, Blood Grouping Reagents, Blood Grouping Substance (FDA Code:
KSX), ...
Maxwin International is a manufacturer, exporter and supplier of diagnostic reagents, rapid cards, laboratory plastic consumables & surgical gauze. Our range includes blood grouping reagent, serology
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FDA Code / Regulation: KSX / 864.9160 Blood group substances of nonhuman origin for in vitro diagnostic use are materials, such as blood group specific substances prepared from nonhuman sources (e.g., pigs, cows, and horses) used to detect, identify, or neutralize antibodies to various human blood group antigens. This generic type of device does not include materials that are licensed by the Center for Biologics Evaluation and Research of the Food and Drug Administration.
Classification. Class II (special controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to 864.9.