Taiwan FDA registration 77b37fead6b5594cc23d81e267f76bc8
“Randox” High Sensitivity CRP Control
TW: “瑞德士”高敏度C反應蛋白品管液
Registration details
- Analysis ID
- 77b37fead6b5594cc23d81e267f76bc8
- License Form
- Ministry of Health Medical Device Import No. 031419
- Customs Code
- DHA05603141900
Company information
- Manufacturer
- RANDOX LABORATORIES LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- KUO'S YUAN IN ENTERPRISE CO., LTD.
Product details
- Intended Use
- This product is used for quality control of accuracy and repeatability of Randox High Sensitivity CRP Assay (model: CP3885).
- 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
- Aug 15, 2018
- Expiry Date
- Aug 15, 2023
About this record
Access comprehensive regulatory information for “Randox” High Sensitivity CRP Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 77b37fead6b5594cc23d81e267f76bc8 and manufactured by RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..
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