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Taifu "Yilicha" AFP test reagent - Taiwan Registration 29a66563e844656b668c87e799012edc

Access comprehensive regulatory information for Taifu "Yilicha" AFP test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 29a66563e844656b668c87e799012edc and manufactured by Taiwan Fu Pharmaceutical Co., Ltd. The authorized representative in Taiwan is Taiwan Fu Pharmaceutical 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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29a66563e844656b668c87e799012edc
Registration Details
Taiwan FDA Registration: 29a66563e844656b668c87e799012edc
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Device Details

Taifu "Yilicha" AFP test reagent
TW: ๅฐๅฏŒ โ€œๆ˜“ๅˆฉๆŸฅโ€AFPๆชข้ฉ—่ฉฆๅŠ‘
Risk Class 2
Cancelled

Registration Details

29a66563e844656b668c87e799012edc

DHY00500197301

Company Information

Taiwan, Province of China

Product Details

Enzyme immunoassay is used to measure the concentration of AFP in human serum as an auxiliary diagnosis for chronic diseases such as hepatitis and liver cirrhosis and primary liver cancer.

C Immunology and microbiology

C.6010 ่…ซ็˜ค็›ธ้—œๆŠ—ๅŽŸๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

Domestic

Dates and Status

Jan 17, 2006

Jan 17, 2016

May 17, 2018

Cancellation Information

Logged out

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