Shared Systems, Inc.

Click Here To EMAIL INQUIRY
Contact: T. S. Enriquez - VP R&D
E-Mail:
Address: PO Box 211587, 3961 Columbia Rd, Augusta, Georgia 30917, USA
Phone: +1-(706)-868-0408, 888-474-2733 | Fax: +1-(706)-855-6588 | Map/Directions >>

Profile: Shared Systems, Inc. is a provider of non-serum based blocking buffers. Our in vitro diagnostic kits include microbiology, serology, HDL cholesterol and infectious disease.

The company was founded in 1991, has revenues of < USD 1 Million and is ISO 9001 certified.

12 Products/Services (Click for related suppliers)

• Bacterial Diagnostic Test

• Cholesterol Colorimetric Test (FDA Code: CGO / 862.1175)

A cholesterol (total) test system is a device intended to measure cholesterol in plasma and serum. Cholesterol measurements are used in the diagnosis and treatment of disorders involving excess cholesterol in the blood and lipid and lipoprotein metabolism disorders.

• Culture Media Quality Control Kit (FDA Code: JTR / 866.2480)

A quality control kit for culture media is a device that consists of paper discs (or other suitable materials), each impregnated with a specified, freeze-dried, viable microorganism, intended for medical purposes to determine if a given culture medium is able to support the growth of that microorganism. The device aids in the diagnosis of disease caused by pathogenic microorganisms and also provides epidemiological information on these diseases.

• Electrodes and Other Components, Gold Cup Electrodes

• Ferrozine Iron Binding Capacity Test (FDA Code: JMO / 862.1415)

An iron-binding capacity test system is a device intended to measure iron-binding capacity in serum. Iron-binding capacity measurements are used in the diagnosis and treatment of anemia.

• HDL Precipitation Method (FDA Code: LBR / 862.1475)

A lipoprotein test system is a device intended to measure lipoprotein in serum and plasma. Lipoprotein measurements are used in the diagnosis and treatment of lipid disorders (such as diabetes mellitus), atherosclerosis, and various liver and renal diseases.

• Infectious Disease Testing Viral Quality Control kits

• LDL & VLDL Precipitation Method (FDA Code: LBR / 862.1475)

• Lipoprotein Low-Density Test System (FDA Code: MRR / 862.1475)

• Negative Control Serological Kit (FDA Code: MJY / 862.1660)

A quality control material (assayed and unassayed) for clinical chemistry is a device intended for medical purposes for use in a test system to estimate test precision and to detect systematic analytical deviations that may arise from reagent or analytical instrument variation. A quality control material (assayed and unassayed) may be used for proficiency testing in interlaboratory surveys. This generic type of device includes controls (assayed and unassayed) for blood gases, electrolytes, enzymes, multianalytes (all kinds), single (specified) analytes, or urinalysis controls.

• Positive Control Serological Kit (FDA Code: MJX / 862.1660)

• Quality Control Kits (FDA Code: JTR / 866.2480)