Pure Global

"Yingfang" Staphylococcus aureus latex reagent (unsterilized) - Taiwan Registration 205636aeacc2a0c22e7ff763f993be3c

Access comprehensive regulatory information for "Yingfang" Staphylococcus aureus latex 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 205636aeacc2a0c22e7ff763f993be3c and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
205636aeacc2a0c22e7ff763f993be3c
Registration Details
Taiwan FDA Registration: 205636aeacc2a0c22e7ff763f993be3c
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Yingfang" Staphylococcus aureus latex reagent (unsterilized)
TW: "็‘ฉ่Šณ" ้‡‘้ปƒ่‰ฒ่‘ก่„็ƒ่Œไนณ่† ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

205636aeacc2a0c22e7ff763f993be3c

Company Information

Taiwan, Province of China

Product Details

It is limited to the first-level identification scope of the "Staphylococcus aureus serum reagent (C.3700)" of the classification and grading management measures for medical devices.

C Immunology and microbiology

C.3700 ้‡‘้ปƒ่‰ฒ่‘ก่„็ƒ่Œ่ก€ๆธ…่ฉฆๅŠ‘

Domestic

Dates and Status

Apr 29, 2011

Apr 29, 2026