Taiwan FDA registration 281ec7255be56140c026347926fc91ff
"Tauns" Capilia Flu Neo Influenza A&B Virus Antigen Rapid Test (Non-Sterile)
TW: "藤司" 流行性感冒病毒A型與B型快速檢測試劑(未滅菌)
Taiwan·Risk Class 1·MD·TAUNS LABORATORIES, INC.·Registered Jun 14, 2016 – Jun 14, 2021ExpiredRegistration details
- Analysis ID
- 281ec7255be56140c026347926fc91ff
- License Form
- Ministry of Health Medical Device Import No. 016643
- Customs Code
- DHA09401664302
Company information
- Manufacturer
- TAUNS LABORATORIES, INC.
- Manufacturer Country
- Japan
- Authorized Representative
- YOULUM BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3330 Influenza virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 14, 2016
- Expiry Date
- Jun 14, 2021
About this record
Access comprehensive regulatory information for "Tauns" Capilia Flu Neo Influenza A&B Virus Antigen Rapid Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 281ec7255be56140c026347926fc91ff and manufactured by TAUNS LABORATORIES, INC.. The authorized representative in Taiwan is YOULUM BIOTECHNOLOGY CO., LTD..
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