Sebia Gel protein electrophoresis detection reagent (unsterilized)
Taiwan·Risk Class 1·SEBIA·Registered Nov 16, 2021 – Nov 16, 2026Active- Analysis ID
- 1d4c762cc4e19e2b3862035b314779b9
- Customs Code
- DHA09402270000
- Manufacturer
- SEBIA
- Manufacturer Country
- France
- Authorized Representative
- ARQon Medtech Co., Ltd.
- Intended Use
- Limited to the first level identification range of the classification and grading management method of medical equipment, protein (chemical separation method) test system (A.1630).
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1630 Protein (Chemical Separation) Test System
- Import Information
- Input;; QMS/QSD
- Registration Date
- Nov 16, 2021
- Expiry Date
- Nov 16, 2026
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Access comprehensive regulatory information for Sebia Gel protein electrophoresis detection reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1d4c762cc4e19e2b3862035b314779b9 and manufactured by SEBIA. The authorized representative in Taiwan is ARQon Medtech Co., Ltd..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SEBIA, and 1 recent registrations in the same category. 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.