Taiwan FDA registration deafab38c3dfdcc045681dd5b711325a
Sebia Hydragel LDL/HDL CHOL Direct (Non-Sterile)
TW: 賽比亞凝膠膽固醇分型電泳試劑(未滅菌)
Registration details
- Analysis ID
- deafab38c3dfdcc045681dd5b711325a
- License Form
- Ministry of Health Medical Device Import No. 019920
- Customs Code
- DHA09401992001
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 "Cholesterol (Total) Test System (A.1175)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1175 Cholesterol (total) test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 12, 2018
- Expiry Date
- Dec 12, 2023
About this record
Access comprehensive regulatory information for Sebia Hydragel LDL/HDL CHOL Direct (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 deafab38c3dfdcc045681dd5b711325a and manufactured by SEBIA. The authorized representative in Taiwan is ARQon Medtech Co., Ltd..
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