Immunochromatographic rapid test for the quantitative detection of cystatin C in whole blood, serum or plasma. Measuring range: 0.1-8 mg/L. Reading time: 10 minutes.
Manufactured by
Alencon, France
VEDALAB is a privately French owned company, founded in 1991 It is devoted to the development, production and marketing of in vitro immunodiagnostic reagents. As a market leader, VEDALAB focuses on international expansion by forming long-term partnerships with reliable and trustworthy distributors worldwide. Continually expanding its impressive range of products, VEDALAB is today the biggest rapid test manufacturer in Europe. VEDALAB s headquarters, its research and development, manufacturing and marketing departments are all located in a modern, well-equipped and expanding (4 500 m²) ISO certified plant in the beautiful Normandy town of Alençon. VEDALAB employs about 50 people all of whom are dedicated to the design, development, manufacture or promotion of a very wide range of innovative reagents and instruments, including the use of patented technologies. Throughout its years of development, VEDALAB has acquired incomparable research experience ranging from initial antibody screening to the creation of its own manufacturing equipment. Such unparalleled experience has made VEDALAB a reference of quality in the world of immunodiagnostics.
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Gentian USA Inc · United States
An in vitro diagnostic reagent for the detection and quantification of cystatin C on clinical chemistry analysers. Used for kidney disease assessment and glomerular filtration rate estimation in clinical laboratories.
Prometheus Bio Inc. · China
Point-of-care rapid test for measuring cystatin C in serum samples. Used as a marker for kidney function assessment and glomerular filtration rate estimation.
NewScen Coast Bio-Pharmaceutical Co., Ltd. · China
A diagnostic test kit for detecting cystatin C using colloidal gold immunochromatographic method. This kit is used for clinical laboratory testing to measure cystatin C levels in patient samples.
Diazyme Laboratories, Inc. · United States
Dual liquid stable latex enhanced immunoturbidimetric method for measuring cystatin C. Provides early detection marker for renal function assessment.
He Bei GuoGao BiotechnoLogy co .,ltd · China
A diagnostic test measuring cystatin C levels for assessment of kidney function. This test provides an alternative marker of glomerular filtration rate and is particularly useful in patients where creatinine-based estimates may be unreliable.
NewScen Coast Bio-Pharmaceutical Co., Ltd. · China
A diagnostic reagent kit for detecting cystatin C using colloidal gold immunochromatography method. This test is used for assessing kidney function and glomerular filtration rate.
Gentian USA Inc · United States
Cystatin C is a superior GFR marker for the diagnosis and therapeutic control of patients of all ages. The Gentian Cystatin C Immunoassay (ERM-DA471/IFCC standardised) is a Particle-Enhanced Turbidimetric Immunoassay (PETIA) for use on a range of clinical chemistry analysers.
Nanjing Leading Medical Technology Co. Ltd. · China
Biochemical reagent for measuring cystatin C levels in serum or urine. Used as a marker for renal function assessment and glomerular filtration rate estimation.
ACTIF CORPORATION CO., LTD · Japan
Cystatin C clinical chemistry reagent using latex turbidimetric method. Used for kidney function assessment and glomerular filtration rate estimation.
Gentian USA Inc · United States
A Particle-Enhanced Turbidimetric Immunoassay (PETIA) for in vitro diagnostic testing of cystatin C in human plasma and serum samples. The assay is used for quantitative determination of cystatin C to assess glomerular filtration rate (GFR) and kidney function in patients of all ages. It is FDA 510(k) cleared, CE-marked, and IVDR certified, with results available in 10 minutes and compatibility with multiple clinical chemistry analyzer platforms including Siemens ADVIA, Abbott ARCHITECT, Beckman Coulter AU, Roche Cobas, and others.
SDIX, LLC · United States
A polyclonal goat antibody against human Cystatin C, IgG fraction purified, for use in in vitro diagnostic reagent formulations. Product code S9123GND0-D0.
PRIMA Lab SA · Switzerland
Rapid self-test for the semi-quantitative detection of C-Reactive Protein (CRP) in whole blood samples
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