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Description: sell igm rapid test kit exemption type africa - PPE ProductsEmergency Use Authorizations FDA. On February 26, 2016, the FDA issued an Emergency Use Authorization (EUA) to authorize the emergency use of Centers for Disease Control and Prevention's (CDC) Zika Immunoglobulin M (IgMPress Releases NovaBayThe fluorecare test kit has been validate ...

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Mar 30, 2020PRESS STATEMENT 30 March 2020 The Food and Drug Administration (FDA) approves the use of five (5) Rapid Test Kits for COVID-19 today, March 30, 2020. The FDA supports all efforts to address this pandemic. These point-of-care test kits are registered for use in countries with reliable regulatory agencies such as China and Singapore. We sell igm rapid test kit certification parameters manilaRead more »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 OKs 5 rapid COVID-19 test kits PhilstarMar 30, 2020Manila HealthTek will sell the remaining kits good for 94,000 test commercially at around P1,300 per kitcheaper than the units currently being used in hospitals which cost about P8,000.

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