Taiwan FDA registration 00a1ebfb49e27ec652b27b271de6289b
"Randox" Liquid Urine Control (Non-Sterile)
TW: "瑞德士" 液態尿液生化品管液 (未滅菌)
Taiwan·Risk Class 1·MD·RANDOX LABORATORIES LTD.·Registered Jul 16, 2018 – Jul 16, 2023ExpiredRegistration details
- Analysis ID
- 00a1ebfb49e27ec652b27b271de6289b
- License Form
- Ministry of Health Medical Device Import No. 019311
- Customs Code
- DHA09401931102
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
- Jul 16, 2018
- Expiry Date
- Jul 16, 2023
About this record
Access comprehensive regulatory information for "Randox" Liquid Urine Control (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 00a1ebfb49e27ec652b27b271de6289b and manufactured by RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..
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