Pf Pan Malaria Antigen Rapid Detection Kit

Description

Malaria Pf/Pan Antigen Rapid Detection Kit is suitable for the qualitative detection of Plasmodium falciparum pf-specific lactate dehydrogenase (Pf-LDH) and Plasmodium panparum pan-specific lactate dehydrogenase (Pan-LDH) in human blood samples in vitro. This product is intended for clinical laboratory personnel who receive specialized instruction and training in the technical aspects of in vitro diagnostic procedures
Malaria Pf/Pan Antigen Rapid Detection Kit This product adopts an immunochromatographic technique and double antibody sandwich method to detect malaria Pf/Pan antigen. This kit does not use an instrument and can produce results when used alone. The product is automatically produced and packaged in a 100,000-level purification workshop, and the shell is sterilized with 75% alcohol.

Specification

Picture details

CE Approved

All our rapid test kits have CE certifications that can be downloaded.

15 types of fast test ce certifications.pdf

Why should use our Pf Pan Malaria?

Malaria Pf Ag Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of Plasmodium falciparum (Pf) specific protein, Histidine-Rich Protein II (FRP-II), in human blood specimens. This device is intended to be used as a screening test and as an aid in the diagnosis of infection with plasmodium. It is suitable for the qualitative detection of Pf-specific lactate dehydrogenase of Plasmodium falciparum (Pf-LDH) and Pan-specific lactate dehydrogenase LDH of Plasmodium panparum (Pan-LDH) in human whole blood samples in vitro.

This Malaria Plasmodium falciparum (P.f.) Rapid Test is a qualitative test for the detection of histidine-rich protein 2 antigen of P.f. in human whole blood. This test is for In-Vitro Diagnostic use only. Collect whole blood into a collection tube (containing EDTA, citrate, or heparin) by venipuncture.

If specimens are not immediately tested, they should be refrigerated at 2-80C. Freezing is recommended if the storage periods are more than 3 days. They should be brought to room temperature before testing. Using the specimen after long-term storage of more than three days can cause a non-specific reaction.

Yongyue Medical Technology (Kunshan) Co., Ltd. is a comprehensive high-tech enterprise integrating R&D, manufacturing, sales, and service, focusing on the third category of medical devices and biomedical consumables (IVD in vitro diagnostic systems). The company is located in the High-tech Zone of Kunshan City, Jiangsu Province, covering an area of ​​nearly 20,000 square meters and a building area of ​​12,000 square meters. The company has completely independent product development, mold making, parts production, and finished product assembly full-process capabilities; it has an independent research and development team, an independent microbiology laboratory, and a physical and chemical laboratory of 10,000 square meters; the production workshop has been built with 5000 square meters and 100,000 Level purification workshop is equipped with nearly 40 imported all-electric injection molding machines and multiple fully automated assembly lines. The company has passed the ISO13485:2016 quality system certification, and the products have passed the EU CE certification. Yongyue Medical Technology takes "caring for human health" as its original intention and "improving the quality of life" as its mission. Adhering to the corporate core values ​​of "caring for life, health-oriented; giving back to the society, cultural inheritance", we will wholeheartedly provide high-quality products and first-class services to the majority of users in the medical and health industry. Yongyue Medical is your partner worthy of trust.