Taiwan FDA registration d38fdc17c1618e24a40a5c18f47a2893
"Randox" RIQAS (Non-Sterile)
TW: "瑞德士" 國際品管評估試劑(未滅菌)
Taiwan·Risk Class 1·MD·RANDOX LABORATORIES LTD.·Registered Nov 15, 2018 – Nov 14, 2023ExpiredRegistration details
- Analysis ID
- d38fdc17c1618e24a40a5c18f47a2893
- License Form
- Ministry of Health Medical Device Import No. 019822
- Customs Code
- DHA09401982201
Company information
- Manufacturer
- RANDOX LABORATORIES LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- KUO'S YUAN IN ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
- 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
- Nov 15, 2018
- Expiry Date
- Nov 14, 2023
About this record
Access comprehensive regulatory information for "Randox" RIQAS (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 d38fdc17c1618e24a40a5c18f47a2893 and manufactured by RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..
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