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"Yingfang" Helicobacter pylori rapid test reagent (unsterilized) - Taiwan Registration ca0d1c07fec57522de7ff83c2aaa8bdf

Access comprehensive regulatory information for "Yingfang" Helicobacter pylori rapid test reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ca0d1c07fec57522de7ff83c2aaa8bdf and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..

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ca0d1c07fec57522de7ff83c2aaa8bdf
Registration Details
Taiwan FDA Registration: ca0d1c07fec57522de7ff83c2aaa8bdf
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Device Details

"Yingfang" Helicobacter pylori rapid test reagent (unsterilized)
TW: "็‘ฉ่Šณ" ๅนฝ้–€่žบๆ—‹ๆกฟ่Œๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

ca0d1c07fec57522de7ff83c2aaa8bdf

Company Information

Taiwan, Province of China

Product Details

Limited to the classification and grading management of medical devices, the first level identification range of "Helicobacter serum reagent (C.0003)".

C Immunology and microbiology

C.0003 ่žบๆ—‹ๆกฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

Domestic

Dates and Status

Jul 15, 2011

Jul 15, 2026