Taiwan FDA registration cc4c3f4e9c463538e96ff3fa79a4632e
Immunotech T-Uptake Reagent Kit (Non-Sterile)
TW: 伊曼紐特克甲狀腺攝取率檢驗試劑組(未滅菌)
Registration details
- Analysis ID
- cc4c3f4e9c463538e96ff3fa79a4632e
- License Form
- Ministry of Health Medical Device Import No. 022428
- Customs Code
- DHA09402242807
Company information
- Manufacturer
- IMMUNOTECH S.R.O.
- Manufacturer Country
- Czechia
- Authorized Representative
- MEGA BONA INTERNATIONAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Triiodothyroxine Absorption Test System (A.1715)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1715 Triiodothyroxine Absorption Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 30, 2021
- Expiry Date
- Mar 30, 2026
About this record
Access comprehensive regulatory information for Immunotech T-Uptake Reagent Kit (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 cc4c3f4e9c463538e96ff3fa79a4632e and manufactured by IMMUNOTECH S.R.O.. The authorized representative in Taiwan is MEGA BONA INTERNATIONAL CO., LTD..
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