Taiwan FDA registration 991564a3fcebde12f8b426d85dd46c2d
AlliedInfo Human Immunodeficiency Virus Type 1 and Type 2 Antibody Enzyme Immunodiagnostic Kit
TW: 聯信人類免疫缺乏病毒1型和2型抗體酵素免疫診斷試劑盒
Registration details
- Analysis ID
- 991564a3fcebde12f8b426d85dd46c2d
- Customs Code
- DHY00500105308
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- YUNG SHIN PHARM. IND. CO., LTD.
Product details
- Intended Use
- Enzyme immunoassay is used to test human serum or plasma for type I and type II antibodies against T-type lymphotropic virus.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Import Information
- Domestic
Dates and status
- Registration Date
- Nov 19, 2003
- Expiry Date
- Jan 11, 2012
- Cancellation Date
- Aug 24, 2011
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for AlliedInfo Human Immunodeficiency Virus Type 1 and Type 2 Antibody Enzyme Immunodiagnostic Kit in Taiwan's medical device market through Pure Global AI's free database. is registered under number 991564a3fcebde12f8b426d85dd46c2d and manufactured by Yongxin Pharmaceutical Industry Co., Ltd. Taichung Lion Factory. The authorized representative in Taiwan is YUNG SHIN PHARM. IND. CO., LTD..
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