Taiwan FDA registration 9636d11dbe87d96f974856d787b3fd8b
Baynex Rapid Test Reagent for Urine Antigen in Veterans Pneumonia
TW: 拜奈克思 退伍軍人肺炎尿液抗原快速檢驗試劑
Taiwan·Risk Class 1·BINAX, INC·Registered Oct 05, 2005 – Oct 05, 2010CancelledRegistration details
- Analysis ID
- 9636d11dbe87d96f974856d787b3fd8b
- Customs Code
- DHA04400076408
Company information
- Manufacturer
- BINAX, INC
- Manufacturer Country
- United States
- Authorized Representative
- Dachen Biotechnology Co., Ltd
Product details
- Intended Use
- 用來定性偵測有肺炎症患者尿液檢中 L.pneumophila serogroup 1 antigen.
- Product Type (Level 1)
- C Immunology and microbiology
- Import Information
- import
Dates and status
- Registration Date
- Oct 05, 2005
- Expiry Date
- Oct 05, 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 Rapid Test Reagent for Urine Antigen in Veterans Pneumonia in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9636d11dbe87d96f974856d787b3fd8b and manufactured by BINAX, INC. The authorized representative in Taiwan is Dachen Biotechnology Co., Ltd.
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