Automated immunoassay analyzer DISKFLU

for clinical diagnosticmicrofluidicfluorescence

Thank you for choosing our Microfluidic Fluorescence Immunoassy (FIA) panel disc Automated Analyzer. Please carefully read the contents of this manual before use. This analyzer has a data storage function inside, and the company is free of responsibility for user losses caused by analyzer damage or data loss, which was caused by user operations. Please do not disassemble or repair the analyzer without authorization, otherwise the post-sales service provided to you will be automatically terminated. Please use the reagents provided by our company, otherwise our company is free of responsibility for the wrong test results. The company has the right to change product design and specifications without prior notice. A slight difference between the picture and the actual product may occur due to the printing process of this manual, please refer to the actual product. You need to ensure that the accessories expansion, re-commissioning or maintenance of the analyzer are carried out by the personnel approved by the company; the relevant electrical equipment conforms to the local standards; the operation is strictly followed to instruction described in this manual. Otherwise, the company is not responsible for the safety, reliability and performance of the device. This manual is formed in accordance to the requirements of EN ISO 15223-1:2016 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements, EN ISO 18113-1:2011 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling)