Fisher Diagnostics

Address: 8365 Valley Pike, Middletown, Virginia 22645, USA
Phone: +1-(800)-524-0294 | Map/Directions >>

Profile: Fisher Diagnostics offers comprehensive contract manufacturing services in diagnostics, biotechnology formulation and packaging. Our blood bank saline is azide-free with no added preservatives, which eliminates preservative-related agglutination and cell washer problems. Its special processing assures extremely low particle count.

The company has revenues of > USD 1 Billion, has ~30500 employees and is ISO certified. NYSE:TMO (SEC Filings)

FDA Registration Number: 1181121

21 Products/Services (Click for related suppliers)  
• Activated Partial Thromboplastin (FDA Code: GFO / 864.7925)
A partial thromboplastin time test is a device used for primary screening for coagulation abnormalities, for evaluation of the effect of therapy on procoagulant disorders, and as an assay for coagulation factor deficiencies of the intrinsic coagulation pathway.
• Antithrombin III Quantitation Test (FDA Code: JBQ / 864.7060)
An antithrombin III assay is a device that is used to determine the plasma level of antithrombin III (a substance which acts with the anticoagulant heparin to prevent coagulation). This determination is used to monitor the administration of heparin in the treatment of thrombosis. The determination may also be used in the diagnosis of thrombophilia (a congenital deficiency of antithrombin III).
• Chemical Supplies
• Coagulation Factor Deficient Plasma (FDA Code: GJT / 864.7290)
A factor deficiency test is a device used to diagnose specific coagulation defects, to monitor certain types of therapy, to detect coagulation inhibitors, and to detect a carrier state (a person carrying both a recessive gene for a coagulation factor deficiency such as hemophilia and the corresponding normal gene).
• Disinfectant Chemical Supply
• Fibrin Split Products (FDA Code: GHH / 864.7320)
A fibrinogen/fibrin degradation products assay is a device used to detect and measure fibrinogen degradation products and fibrin degradation products (protein fragments produced by the enzymatic action of plasmin on fibrinogen and fibrin) as an aid in detecting the presence and degree of intravascular coagulation and fibrinolysis (the dissolution of the fibrin in a blood clot) and in monitoring therapy for disseminated intravascular coagulation (nonlocalized clotting in the blood vessels).
• Fibrinogen Control Plasma (FDA Code: GIL / 864.7340)
A fibrinogen determination system is a device that consists of the instruments, reagents, standards, and controls used to determine the fibrinogen levels in disseminated intravascular coagulation (nonlocalized clotting within the blood vessels) and primary fibrinolysis (the dissolution of fibrin in a blood clot).
• Fibrinogen Determination System Test (FDA Code: KQJ / 864.7340)
• Fibrinogen Standard (FDA Code: GFX / 864.7340)
• Fibrinogen Test (FDA Code: GIS / 864.7340)
• General Diagnostic Supplies
• General Medical Supplies
• Heparin (FDA Code: IAZ / 864.4400)
Enzyme preparations are products that are used in the histopathology laboratory for the following purposes:
• Heparin Assay (FDA Code: KFF / 864.7525)
A heparin assay is a device used to determine the level of the anticoagulant heparin in the patient's circulation. These assays are quantitative clotting time procedures using the effect of heparin on activated coagulation factor X (Stuart factor) or procedures based on the neutralization of heparin by protamine sulfate (a protein that neutralizes heparin).
• Hospital Chemical Supply
• Lab Chemical Supply
• Multi Analyte Mixture - Calibrator (FDA Code: JIX / 862.1150)
A calibrator is a device intended for medical purposes for use in a test system to establish points of reference that are used in the determination of values in the measurement of substances in human specimens. (See also 862.2 in this part.)
• Plasma Coagulation Control (FDA Code: GGN / 864.5425)
A multipurpose system for in vitro coagulation studies is a device consisting of one automated or semiautomated instrument and its associated reagents and controls. The system is used to perform a series of coagulation studies and coagulation factor assays.
• Prothrombin Time Test (FDA Code: GJS / 864.7750)
A prothrombin time test is a device used as a general screening procedure for the detection of possible clotting factor deficiencies in the extrinsic coagulation pathway, which involves the reaction between coagulation factors III and VII, and to monitor patients receiving coumarin therapy (the administration of one of the coumarin anticoagulants in the treatment of venous thrombosis or pulmonary embolism).
• Sickle Cell Test (FDA Code: GHM / 864.7825)
A sickle cell test is a device used to determine the sickle cell hemoglobin content of human blood to detect sickle cell trait or sickle cell diseases.
• Stain Sets & Solutions

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