Taiwan FDA registration f18b1171d865c33824172210c6a5ab6d
SEBIA MINICAP CDT (Non-Sterile)
TW: 賽比亞 迷你型毛細管缺醣攜鐵蛋白檢測試劑 (未滅菌)
Taiwan·Risk Class 1·MD·SEBIA·Registered Jan 18, 2021 – Jan 18, 2026ExpiredRegistration details
- Analysis ID
- f18b1171d865c33824172210c6a5ab6d
- License Form
- Ministry of Health Medical Device Import No. 022252
- Customs Code
- DHA09402225209
Company information
- Manufacturer
- SEBIA
- Manufacturer Country
- France
- Authorized Representative
- ARQon Medtech Co., Ltd.
Product details
- Intended Use
- Limited to the first level identification range of the measures for the administration of medical devices "r-glutamyl transferase (GGT) and isoenzyme test system (A.1360)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1360 r-glutamyl transferase (GGT) and isoenzyme test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 18, 2021
- Expiry Date
- Jan 18, 2026
About this record
Access comprehensive regulatory information for SEBIA MINICAP CDT (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f18b1171d865c33824172210c6a5ab6d and manufactured by SEBIA. The authorized representative in Taiwan is ARQon Medtech Co., Ltd..
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