One more YHLO - Beckman Coulter joint automation system installed
Time Posted ：2024-04-03
Recently, another installation of YHLO iModules system with Beckman Coulter Power Express clinical lab automation systems was perfectly completed in the Sixth Hospital of Wuhan, Hubei Province, China. This integrated Total Laboratory Automation (TLA) will boost the efficiency of daily workload in the hospital's laboratory.
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Great inheritance of YHLO iFlash Series, new product being installed
Time Posted ：2024-04-03
The newly launched YHLO iFlash family member, iFlash 9000, has caught much attention in China’s in vitro diagnostic market. In only a few days after launching, the first iFlash 9000 has been successfully installed and put into operation in a large class A hospital in Jiangsu Province, China.
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YHLO Showcased Its Latest iFlash CLIA at MEDICA 2021
Time Posted ：2024-04-03
From 15-18 November, YHLO is making a grand exposure at MEDICA 2021, with its latest chemiluminescence immunoassay (CLIA) analyzer iFlash 1200, the bench-top analyzer iFlash 1800, the mono-test CLIA analyzer iStar 500, and total solutions for SARS-CoV-2 on exhibition.
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World Pneumonia Day
Time Posted ：2024-04-03
World Pneumonia Day provides an annual forum for the world to stand together and demand action in the fight against pneumonia. More than 100 organizations representing the interests of children joined forces as the Global Coalition against Child Pneumonia
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EU COVID-19 Rapid Antigen Tests Common List Inclusion of YHLO GLINE-2019-nCoV Ag
Time Posted ：2024-04-03
After being successfully granted official approval by the German PEI, YHLO’s rapid antigen test product GLINE-2019-nCoV Ag is officially listed on the EU COVID-19 Rapid Antigen Tests Common List on 8th December, 2021.
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YHLO Receives FDA 510(K) Clearance for iFlash 1800 Chemiluminescence Immunoassay Analyzer and iFlash Total βhCG Assay
Time Posted ：2024-04-03
YHLO Biotech announced today that the iFlash 1800 Chemiluminescence Immunoassay Analyzer and iFlash Total βhCG Assay have received a 510(k) clearance from the U.S. Food and Drug Administration through a local partner. A 510(K) is a premarket submission made to FDA to demonstrate that the device to be marketed is as safe and effective, that is, substantially equivalent as predicate device. Receiving the 510(K) expands YHLO’s reach of iFlash 1800, as it has been installed in nearly 100 counties globally.
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Congrats! YHLO Received CE mark on COVID-19 Ag Self-Test Kit
Time Posted ：2024-04-03
Recently, YHLO proudly announced that the COVID-19 self-test kit, GLINE-2019-nCoV Ag, has received the EC Certificate from the Polish Centre for Testing and Certification (POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A.).
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YHLO COVID-19 Rapid Ag Test Kits(self-test) Approved by BfArM
Time Posted ：2024-04-03
YHLO COVID-19 self-test kit, GLINE-2019-nCoV Ag assay was granted special approval by the German Federal Institute for Drugs and Medical Devices (BfArM) in Germany.
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Add: Building 1, YHLO Biopark, Baolong 2nd Road, Baolong Subdistrict, Longgang District, 518116 Shenzhen, P.R.China
