Taiwan FDA registration 9a1d21499fb5f9ddc29fe1feb5ee3944
"Randox" International Quality Assessment Scheme (RIQAS) (Non-Sterile)
TW: "倫多" 國際能力試驗計畫(未滅菌)
Taiwan·Risk Class 1·MD·RANDOX LABORATORIES LTD.·Registered May 23, 2018 – May 23, 2028ActiveRegistration details
- Analysis ID
- 9a1d21499fb5f9ddc29fe1feb5ee3944
- License Form
- Ministry of Health Medical Device Import No. 019081
- Customs Code
- DHA09401908101
Company information
- Manufacturer
- RANDOX LABORATORIES LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EUGENE-CHEN 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
- May 23, 2018
- Expiry Date
- May 23, 2028
About this record
Access comprehensive regulatory information for "Randox" International Quality Assessment Scheme (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 9a1d21499fb5f9ddc29fe1feb5ee3944 and manufactured by RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is EUGENE-CHEN CO., LTD..
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