Taiwan FDA registration e40e999f7d324fe7401518783afce8fb
"Bexister" uric acid detection reagent (sterilized)
TW: "百希斯特" 尿酸檢測試劑 (滅菌)
Taiwan·Risk Class 1·BIOSYSTEMS S.A.·Registered Sep 25, 2013 – Sep 25, 2018CancelledRegistration details
- Analysis ID
- e40e999f7d324fe7401518783afce8fb
- Customs Code
- DHA09401344802
Company information
- Manufacturer
- BIOSYSTEMS S.A.
- Manufacturer Country
- Spain
- Authorized Representative
- HONEST MEDICAL INC.
Product details
- Intended Use
- Limited to the first level identification range of the "uric acid test system (A.1775)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1775 尿酸試驗系統
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Sep 25, 2013
- Expiry Date
- Sep 25, 2018
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bexister" uric acid detection reagent (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e40e999f7d324fe7401518783afce8fb and manufactured by BIOSYSTEMS S.A.. The authorized representative in Taiwan is HONEST MEDICAL INC..
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