Aalto Scientific Ltd

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Web: http://www.aaltoscientific.com
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Address: 1959 Kellogg Ave, Carlsbad, California 92008, USA
Phone: +1-(800)-748-6674 | Fax: +1-(760)-431-6942 | Map/Directions >>

Profile: Aalto Scientific Ltd manufactures human sera. We supply human cardiac antigens, creatine kinase MM, MB and BB.

The company was founded in 1979, has revenues of USD 1-5 Million, has ~20 employees and is ISO 9001 certified.

FDA Registration Number: 3011325031

12 Products/Services (Click for related suppliers)

• Alcohol Control Materials (FDA Code: DKC / 862.3280)

A clinical toxicology control material is a device intended to provide an estimation of the precision of a device test system and to detect and monitor systematic deviations from accuracy resulting from reagent or instrument defects. This generic type of device includes various single, and multi-analyte control materials.

• Assayed and Unassayed Single (Specified) Analyte Controls (FDA Code: JJX / 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.

• Complement Protein (FDA Code: DHL / 866.4100)

A complement reagent is a device that consists of complement, a naturally occurring serum protein from any warm-blooded animal such as guinea pigs, that may be included as a component part of serological test kits used in the diagnosis of disease.

• Drug Mixture Control Materials (FDA Code: DIF / 862.3280)

• Electrolyte Control (FDA Code: JJR / 862.1660)

• Enzyme Controls (FDA Code: JJT / 862.1660)

• Fertility Products, Serum Protein Substitute

• Hematocrit Control (FDA Code: GLK / 864.8625)

A hematology quality control mixture is a device used to ascertain the accuracy and precision of manual, semiautomated, and automated determinations of cell parameters such as white cell count (WBC), red cell count (RBC), platelet count (PLT), hemoglobin, hematocrit (HCT), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), and mean corpuscular hemoglobin concentration (MCHC).

• Hematology Quality Control Mixture (FDA Code: JPK / 864.8625)

• Multi Analyte Control (FDA Code: JJY / 862.1660)

• Production Raw Material

• Qualitative and Quantitative Factor Deficiency Test (FDA Code: GGP / 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).