Immunochromatographic rapid test for the quantitative detection of AFP (alpha-fetoprotein) in whole blood, serum or plasma. Measuring range: 10–300 ng/mL. Reading time: 10 minutes.
Manufactured by
VEDALAB SAS
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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MedLevensohn · Brazil
A rapid diagnostic test for detecting alpha-fetoprotein (AFP), a tumor marker used in cancer screening and diagnosis.
Zhuhai Encode Medical Engineering Co Ltd · China
Quantitative immunofluorescence-based rapid test for precise measurement of analytes in clinical specimens. Combines fluorescence detection with rapid testing methodology for accurate results. Suitable for various immunological assessments in diagnostic laboratories.
HANGZHOU LAIHE BIOTECH CO.,LTD · China
Rapid screening assays for AFP, CEA, PSA, and other key oncology markers enabling accessible, early-stage risk stratification in community health screening and specialist oncology settings. Offers quantitative fluorescence and semi-quantitative formats with low sample volume requirements of 50–100 µL serum/plasma. Multi-marker combo panels are available.
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