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"Wanfu" Helicobacter pylori test kit (serum/plasma) (unsterilized) - Taiwan Registration f491e219cf71601eeb5c96d8d2cc87a2

Access comprehensive regulatory information for "Wanfu" Helicobacter pylori test kit (serum/plasma) (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f491e219cf71601eeb5c96d8d2cc87a2 and manufactured by GUANGZHOU WONDFO BIOTECH CO., LTD.. The authorized representative in Taiwan is HUNGAN MEDICAL CO..

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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f491e219cf71601eeb5c96d8d2cc87a2
Registration Details
Taiwan FDA Registration: f491e219cf71601eeb5c96d8d2cc87a2
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Device Details

"Wanfu" Helicobacter pylori test kit (serum/plasma) (unsterilized)
TW: โ€œ่ฌ็ฆโ€ ๅนฝ้–€่žบๆ—‹ๆกฟ่Œๆชขๆธฌ่ฉฆๅŠ‘็›’(่ก€ๆธ…/่ก€ๆผฟ) (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

f491e219cf71601eeb5c96d8d2cc87a2

DHA09600407807

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‘

Chinese goods;; input

Dates and Status

Jan 20, 2020

Jan 20, 2025