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Across the Ocean Exhibition Style丨 Synthgene made a wonderful appearance at the 2022 AACC Expo in the United States!
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2022
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Synthgene will meet you in 2022 American AACC
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Synthgene's 3 monkeypox virus detection kits have also been approved by the EU CE certification
On May 24, Nanjing Synthgene Medical Technology Co., Ltd.. (hereinafter referred to as "Synthgene") developed products "Monkeypox Virus Nucleic Acid Detection Kit (RT-PCR Method)", Monkeypox Virus Antigen Detection Kit (Colloidal Gold Method) ), monkeypox virus antibody detection kit (colloidal gold method) three products have obtained EU CE certificate at the same time, the approval of this series of products means that these kits can be sold in EU countries and countries that recognize EU CE certification, and can further It broadens the application fields of the company's products and responds more comprehensively to the needs of overseas markets.
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SARS-CoV-2 Nucleocapsid (N) Antigen Rapid Detection Kit obtained EU CE self-test certificate
At present, the SARS-CoV-2-related testing products independently developed and produced by Synthgene have been sold in more than 30 overseas countries, and were approved by the State Food and Drug Administration on April 1, 2022 (Registration Certificate No.: National Machinery Note 20223400427), officially launched!
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Help fight the epidemic! Synthgene donates SARS-CoV-2 Antigen Rapid Detection Kit to Nanjing University
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