Taiwan FDA registration 19bb1573572847aaae8b1b6d0001e81a
“Sebia” Hypergamma Control
TW: “賽比亞” 高濃度伽馬蛋白電泳品管液
Taiwan·Risk Class 2·MD·SEBIA·Registered Feb 07, 2017 – Feb 07, 2027ActiveRegistration details
- Analysis ID
- 19bb1573572847aaae8b1b6d0001e81a
- License Form
- Ministry of Health Medical Device Import No. 029320
- Customs Code
- DHA05602932002
Company information
- Manufacturer
- SEBIA
- Manufacturer Country
- France
- Authorized Representative
- ARQon Medtech Co., Ltd.
Product details
- Intended Use
- This product is used on HYDRAGEL, CAPILLARYS and MINICAP and other instruments as a quality control substance for human serum protein electrophoresis quantitative test.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 07, 2017
- Expiry Date
- Feb 07, 2027
About this record
Access comprehensive regulatory information for “Sebia” Hypergamma Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 19bb1573572847aaae8b1b6d0001e81a and manufactured by SEBIA. The authorized representative in Taiwan is ARQon Medtech Co., Ltd..
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