CORPORATE: CLIAwaived.com
11578 Sorrento Valley Road
Suite 25/26
San Diego, CA 92121
858-481-5031 tel
801-720-7568 fax SALES: Toll
Free 1-888-882-7739 info@cliawaived.com
Chemcard Total Cholesterol Test
Chemcard Total Cholesterol Test CHEM-43024-24 (24 Tests) Chemcard Cholesterol test kit, is a non instrumented, 3 minute test intended for use for early detection of elevated blood cholesterol levels associated with increased risk of coronary artery disease. The Chemcard uses a single drop of whole blood. (NOTE: Due to FDA restrictions, the Chemcard Cholesterol Test is available for use in the US by medical professionals only!) For in vitro diagnostic use only.
The Chemcard Cholesterol test is a complete, disposable, 3 minute test intended for use for early detection of elevated blood cholesterol levels associated with increased risk of coronary artery disease. The National Heart, Lung and Blood Institute's National Cholesterol Education Program classifies cardiac risk level based on total cholesterol concentration as follows:
Less than 200 mg/dL (5.2 mmol/l) - DESIRABLE blood cholesterol.
200 to 239 mg/dL (5.2 to 6.2 mmol/l) - BORDERLINE HIGH blood cholesterol.
240 mg/dL (6.2 mmol/l) or above - HIGH blood cholesterol.
The Chemcard offers unsurpassed simplicity for instant determination of total cholesterol concentration in the diagnostically critical range of 150 to 300 mg/d: (3.9 to 7.8 mmol/l). The Chemcard uses a single drop of whole blood from a fingerstick to provide a semi-quantitative estimate of total cholesterol concentration without the use of an instrument, centrifuge or sample measurement. Results are interpreted after 3 minutes by matching color with one of the six color blocks calibrated in 25 mg/dL increments. The Chemcard is the simplest, most cost effective cholesterol screening device available.
Due to FDA restrictions, the Chemcard Cholesterol Test is available for use in the US by medical professionals only.
The Chemcard Cholesterol Test is CE marked for self-testing in the European Union under Annex IV, Article 3 of EC Directive 98/79/EC on IN VITRO Diagnostic Medical Devices.
