Pure Global

"Yingfang" Aspergillus pylori urease test set (unsterilized) - Taiwan Registration fa0cc804d250d0e14afc4e633c13fa0c

Access comprehensive regulatory information for "Yingfang" Aspergillus pylori urease test set (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fa0cc804d250d0e14afc4e633c13fa0c and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is Yingfang Co., Ltd. Taichung Factory.

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
fa0cc804d250d0e14afc4e633c13fa0c
Registration Details
Taiwan FDA Registration: fa0cc804d250d0e14afc4e633c13fa0c
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Yingfang" Aspergillus pylori urease test set (unsterilized)
TW: "็‘ฉ่Šณ" ๅนฝ้–€ๆ›ฒ็‹€ๆกฟ่Œๅฐฟ็ด ้…ถๆธฌ่ฉฆ็ต„ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

fa0cc804d250d0e14afc4e633c13fa0c

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

Apr 22, 2011

Apr 22, 2026