Taiwan FDA registration c4771d1ca854d4adcb1eabb790f7a664
Meis Substance Abuse Test Liquid Quality Control Group
TW: 麥斯藥物濫用檢測液狀品管組
Taiwan·Risk Class 2·MICROGENICS CORPORATION·Registered Dec 10, 2020 – Dec 10, 2025ExpiredRegistration details
- Analysis ID
- c4771d1ca854d4adcb1eabb790f7a664
- Customs Code
- DHA05603416701
Company information
- Manufacturer
- MICROGENICS CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- THERMO FISHER SCIENTIFIC TAIWAN CO., LTD.
Product details
- Intended Use
- This product is used as a quality control solution for semi-quantitative and qualitative analysis of drugs and drug metabolites using the patient's urine as a sample.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Dec 10, 2020
- Expiry Date
- Dec 10, 2025
About this record
Access comprehensive regulatory information for Meis Substance Abuse Test Liquid Quality Control Group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c4771d1ca854d4adcb1eabb790f7a664 and manufactured by MICROGENICS CORPORATION. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC TAIWAN CO., LTD..
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