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Description: FDA Advisory No. 2020-483 |FDA APPROVES RAPID …Mar 30, 2020In line with the ongoing response to the increasing number of COVID-19 cases in the Philippines, the Food and Drug Administration (FDA)- Philippines hereby provides an initial list of approved Rapid Antibody Test Kits. PRODUCT NAME MANUFACTURER 1. NANJING VAZYME 2019-nCoV IgG/IgM DETECTION KIT Biolidics Limite ...

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The COVID-19 IgG/IgM Rapid Test Device is intended for use with human whole blood, serum or plasma specimens only. Only clear, non-hemolyzed specimens are recommended for use with this test. Serum or plasma should be separated as soon as possible to avoid hemolysis.COVID-19 for Laboratories - CDPH HomeCDPH warns consumers against use of COVID-19 tests not approved by the U.S. Food and Drug Administration (FDA) Most of the tests currently used to detect SARS-CoV-2, the virus that causes COVID-19 disease, by the State Public Health Laboratory, local public health laboratories, and licensed commercial laboratories are molecular polymerase chain reaction (PCR) tests.Carolina Liquid Chemistries Clinical Chemistry Analyzers sell philippines certification igm rapid test kitCLC Now Offers COVID-19 Rapid Screen Antibody Test GREENSBORO, NC (March 27, 2020) Carolina Liquid Chemistries, Corp. (CLC), an innovative biotechnology company, now offers the AllTest 2019-nCoV IgG/IgM Rapid Screen Antibody Test Cassette in accordance with Sections C and D of the

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FDA Advisory No. 2020-483 |FDA APPROVES RAPID

Mar 30, 2020In line with the ongoing response to the increasing number of COVID-19 cases in the Philippines, the Food and Drug Administration (FDA)- Philippines hereby provides an initial list of approved Rapid Antibody Test Kits. PRODUCT NAME MANUFACTURER 1. NANJING VAZYME 2019-nCoV IgG/IgM DETECTION KIT Biolidics Limited. 37 Jalan Pemimpin, #02-07, Mapex, Singapore 2.FDA EUA Authorized (COVID-19) Instant Test Confirm sell philippines certification igm rapid test kitCOVID-19 IgG/IgM Rapid Test Cassette. The Novel Coronavirus testing kit manufactured by Healgen Scientific LLC is conducted by using whole blood/serum/plasma and placing it in the center well of the cassette and then adding two drops of the buffer to the buffer well labeled B. Results should appear within 10 minutes and are invalid after 15 minutes.FDA OKs 5 rapid COVID-19 test kits PhilstarMar 30, 2020MANILA, Philippines (Update 1:57 p.m.) The country's Food and Drug Administration approved the use of five rapid test kits for the new coronavirus as

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