Taiwan FDA registration d178b28a928dee7a0fbd7152a4c05572
"Bexister" inorganic phosphorus detection reagent (sterilization)
TW: "百希斯特"無機磷檢測試劑(滅菌)
Taiwan·Risk Class 1·BIOSYSTEMS S.A.·Registered Sep 27, 2013 – Sep 27, 2018CancelledRegistration details
- Analysis ID
- d178b28a928dee7a0fbd7152a4c05572
- Customs Code
- DHA09401345601
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 Measures for the Administration of Medical Devices "Phosphorous Acid (Inorganic) Test System (A.1580)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1580 Phosphoric acid (inorganic) test system
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Sep 27, 2013
- Expiry Date
- Sep 27, 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" inorganic phosphorus detection reagent (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d178b28a928dee7a0fbd7152a4c05572 and manufactured by BIOSYSTEMS S.A.. The authorized representative in Taiwan is HONEST MEDICAL INC..
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