Taiwan FDA registration 29a66563e844656b668c87e799012edc
Taifu "Yilicha" AFP test reagent
TW: 台富 “易利查”AFP檢驗試劑
Taiwan·Risk Class 2·Taiwan Fu Pharmaceutical Co., Ltd·Registered Jan 17, 2006 – Jan 17, 2016CancelledRegistration details
- Analysis ID
- 29a66563e844656b668c87e799012edc
- Customs Code
- DHY00500197301
Company information
- Manufacturer
- Taiwan Fu Pharmaceutical Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Taiwan Fu Pharmaceutical Co., Ltd
Product details
- Intended Use
- 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.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.6010 腫瘤相關抗原免疫試驗系統
- Import Information
- Domestic
Dates and status
- Registration Date
- Jan 17, 2006
- Expiry Date
- Jan 17, 2016
- Cancellation Date
- May 17, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
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.
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