Taiwan FDA registration d0c102b53f0f1f73921ec206ca9633e4
Baynexus Streptococcus pneumoniae urine antigen rapid test reagent
TW: 拜奈克思肺炎鏈球菌尿液抗原快速檢驗試劑
Taiwan·Risk Class 1·BINAX, INC·Registered Oct 24, 2005 – Oct 24, 2010CancelledRegistration details
- Analysis ID
- d0c102b53f0f1f73921ec206ca9633e4
- Customs Code
- DHA04400117102
Company information
- Manufacturer
- BINAX, INC
- Manufacturer Country
- United States
- Authorized Representative
- Dachen Biotechnology Co., Ltd
Product details
- Intended Use
- Urine or cerebrospinal fluid is used as a test to detect the antigen of Chaincoccus pneumoniae.
- Product Type (Level 1)
- C Immunology and microbiology
- 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 Baynexus Streptococcus pneumoniae urine 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 d0c102b53f0f1f73921ec206ca9633e4 and manufactured by BINAX, INC. The authorized representative in Taiwan is Dachen Biotechnology Co., Ltd.
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