Taiwan FDA registration c0c850965733b38abe7fa0bcd41e2a2a
Baynex Influenza 2-in-1 Viral Antigen Rapid Test Reagent
TW: 拜奈克思流行性感冒二合一型病毒抗原快速檢驗試劑
Taiwan·Risk Class 1·BINAX, INC·Registered Oct 24, 2005 – Oct 24, 2010CancelledRegistration details
- Analysis ID
- c0c850965733b38abe7fa0bcd41e2a2a
- Customs Code
- DHA04400117201
Company information
- Manufacturer
- BINAX, INC
- Manufacturer Country
- United States
- Authorized Representative
- Dachen Biotechnology Co., Ltd
Product details
- Intended Use
- It is used in serum tests to identify antibodies to cold viruses in serum.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3330 流感病毒血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Oct 24, 2005
- Expiry Date
- Oct 24, 2010
- Cancellation Date
- Nov 06, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Baynex Influenza 2-in-1 Viral Antigen Rapid Test Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c0c850965733b38abe7fa0bcd41e2a2a and manufactured by BINAX, INC. The authorized representative in Taiwan is Dachen Biotechnology Co., Ltd.
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