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"Aiwe" Helicobacter pylori rapid test reagent (unsterilized) - Taiwan Registration 5257d8bbcb1cf3cfb5efa8c4f7d135a0

Access comprehensive regulatory information for "Aiwe" 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 5257d8bbcb1cf3cfb5efa8c4f7d135a0 and manufactured by AVE SCIENCE & TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is DiaTech Technology Co., Ltd..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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5257d8bbcb1cf3cfb5efa8c4f7d135a0
Registration Details
Taiwan FDA Registration: 5257d8bbcb1cf3cfb5efa8c4f7d135a0
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Device Details

"Aiwe" Helicobacter pylori rapid test reagent (unsterilized)
TW: โ€œๆ„›ๅจโ€ ๅนฝ้–€่žบๆ—‹ๆกฟ่Œๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

5257d8bbcb1cf3cfb5efa8c4f7d135a0

DHA09600430202

Company Information

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‘

Input;; Chinese goods

Dates and Status

Aug 31, 2020

Aug 31, 2025