Saibia Gel Urine Protein Electrophoresis Test Reagent (Unsterilized)
- Analysis ID
- be00cfcff87ce02d32a57cd3c32893d7
- Customs Code
- DHA09402259003
- 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
- Jul 30, 2021
- Expiry Date
- Jul 30, 2026
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Access comprehensive regulatory information for Saibia Gel Urine Protein Electrophoresis Test 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 be00cfcff87ce02d32a57cd3c32893d7 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.