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)
Taiwan flagTaiwan·Risk Class 1·MD·IMMUNOTECH S.R.O.·Registered Mar 30, 2021 – Mar 30, 2026Expired
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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