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"Sekisui" Trichomonas. V Ag Rapid Test Kit (Non-Sterile) - Taiwan Registration f4a66ca1a457ef72ee7c54c124dd8a9b

Access comprehensive regulatory information for "Sekisui" Trichomonas. V Ag Rapid Test Kit (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f4a66ca1a457ef72ee7c54c124dd8a9b and manufactured by SEKISUI DIAGNOSTICS, LLC. The authorized representative in Taiwan is ARSENALS IVD CO., LTD..

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f4a66ca1a457ef72ee7c54c124dd8a9b
Registration Details
Taiwan FDA Registration: f4a66ca1a457ef72ee7c54c124dd8a9b
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Device Details

"Sekisui" Trichomonas. V Ag Rapid Test Kit (Non-Sterile)
TW: "็ธพ็ฉ—" ้™ฐ้“ๆปด่Ÿฒๆชขๆธฌ่ฉฆๅŠ‘็›’ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

f4a66ca1a457ef72ee7c54c124dd8a9b

Ministry of Health Medical Device Import No. 017391

DHA09401739103

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".

C Immunology and microbiology devices

C2660 Microbial identification and assay equipment

Imported from abroad

Dates and Status

Jan 09, 2017

Jan 09, 2027