Taiwan FDA registration f093f8d6043fd1dfa3ac0c21387e8b83
SEBIA CAPI 3 Urine (Non-Sterile)
TW: 賽比亞第三代毛細管尿蛋白電泳套組 (未滅菌)
Taiwan·Risk Class 1·MD·SEBIA·Registered May 31, 2019 – May 31, 2024ExpiredRegistration details
- Analysis ID
- f093f8d6043fd1dfa3ac0c21387e8b83
- License Form
- Ministry of Health Medical Device Import No. 020510
- Customs Code
- DHA09402051008
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 "Protein (Chemical Separation Method) Test System (A.1630)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1630 Protein (Chemical Separation) Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 31, 2019
- Expiry Date
- May 31, 2024
About this record
Access comprehensive regulatory information for SEBIA CAPI 3 Urine (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 f093f8d6043fd1dfa3ac0c21387e8b83 and manufactured by SEBIA. The authorized representative in Taiwan is ARQon Medtech Co., Ltd..
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