Taiwan FDA registration 5e92e3fe9215d23cd0f9df463d7b19ca
"Bexister" microprotein detection reagent (sterilization)
TW: "百希斯特"微蛋白檢測試劑(滅菌)
Registration details
- Analysis ID
- 5e92e3fe9215d23cd0f9df463d7b19ca
- Customs Code
- DHA09401345802
Company information
- Manufacturer
- BIOSYSTEMS S.A.
- Manufacturer Country
- Spain
- Authorized Representative
- HONEST MEDICAL INC.
Product details
- Intended Use
- Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Urine Protein or Albumin (Non-quantitative) Test System (A.1645)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1645 Urine protein or albumin (non-quantitative) testing system
- Import Information
- Input;; QMS/QSD
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" microprotein 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 5e92e3fe9215d23cd0f9df463d7b19ca and manufactured by BIOSYSTEMS S.A.. The authorized representative in Taiwan is HONEST MEDICAL INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices