Ids Limited

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Web: http://www.idsltd.com
E-Mail:
Address: Boldon Business Park, Boldon, Tyne and Wear, England NE359PD, United Kingdom
Phone: +44-(191)-5190660 | Fax: +44-(191)-5190760 | Map/Directions >>

Profile: Ids Limited develops assays for use in clinical and research laboratories. We are an ISO 9001, ISO 9002 certified company. We offer products like Alk-Phos Mab, biotin Mab, ADG RIA & Albumin. Our DRG AFP MTPL enzyme immuno assay helps in the quantitative determination of alpha-fetoprotein in serum and amniotic fluid. The IDS 25-hydroxy vitamin D kit is a conventional liquid phase radioimmunoassay intended for the quantitative determination of 25-hydroxy vitamin D (25-OHD) and other hydroxylated metabolites in human serum or plasma.

The company has revenues of USD 1-5 Million, has ~30 employees and is ISO 9001, ISO 9002 certified.

FDA Registration Number: 3012639861
US Agent: Sean Lee / Ids Innovative Lasers Usa
Phone: +1-(913)-200-8711 E-Mail:

11 Products/Services (Click for related suppliers)

• Alkaline Phosphatase Isoenzymes Electrophoretic Separation Test (FDA Code: CIN / 862.1050)

An alkaline phosphatase or isoenzymes test system is a device intended to measure alkaline phosphatase or its isoenzymes (a group of enzymes with similar biological activity) in serum or plasma. Measurements of alkaline phosphatase or its isoenzymes are used in the diagnosis and treatment of liver, bone, parathyroid, and intestinal diseases.

• 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.

• Discrete Photometric Chemistry Analyzer (FDA Code: JJE / 862.2160)

A discrete photometric chemistry analyzer for clinical use is a device intended to duplicate manual analytical procedures by performing automatically various steps such as pipetting, preparing filtrates, heating, and measuring color intensity. This device is intended for use in conjunction with certain materials to measure a variety of analytes. Different models of the device incorporate various instrumentation such as micro analysis apparatus, double beam, single, or dual channel photometers, and bichromatic 2-wavelength photometers. Some models of the device may include reagent-containing components that may also serve as reaction units.

• Human Growth Hormone Radioimmunoassay (FDA Code: CFL / 862.1370)

A human growth hormone test system is a device intended to measure the levels of human growth hormone in plasma. Human growth hormone measurements are used in the diagnosis and treatment of disorders involving the anterior lobe of the pituitary gland.

• Hydroxyproline Chromatography Column Test (FDA Code: JMM / 862.1400)

A hydroxyproline test system is a device intended to measure the amino acid hydroxyproline in urine. Hydroxyproline measurements are used in the diagnosis and treatment of various collagen (connective tissue) diseases, bone disease such as Paget's disease, and endocrine disorders such as hyperparathyroidism and hyperthyroidism.

• Iso-Insulin

• Iso-Insulin EIA Diabetes and Obesity Markers

• Osteocalcin Test System (FDA Code: NEO / 862.1050)

• Parathyroid Hormone Radioimmunoassay Test (FDA Code: CEW / 862.1545)

A parathyroid hormone test system is a device intended to measure the levels of parathyroid hormone in serum and plasma. Measurements of parathyroid hormone levels are used in the differential diagnosis of hypercalcemia (abnormally high levels of calcium in the blood) and hypocalcemia (abnormally low levels of calcium in the blood) resulting from disorders of calcium metabolism.

• Radioimmunoassay Test

• Vitamin D Test System (FDA Code: MRG / 862.1825)

A vitamin D test system is a device intended for use in clinical laboratories for the quantitative determination of 25-hydroxyvitamin D (25-OH-D) and other hydroxylated metabolites of vitamin D in serum or plasma to be used in the assessment of vitamin D sufficiency.