Taiwan FDA registration e411d323221d38b6fe9d8a2206193415
“Medica” Creatinine Reagent Kit
TW: “美麗佳” 肌酸酐試劑
Taiwan·Risk Class 2·MD·MEDICA CORPORATION·Registered Apr 08, 2014 – Apr 08, 2024ExpiredRegistration details
- Analysis ID
- e411d323221d38b6fe9d8a2206193415
- License Form
- Ministry of Health Medical Device Import No. 025937
- Customs Code
- DHA05602593700
Company information
- Manufacturer
- MEDICA CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- GRAND MARQUIS CO., LTD.
Product details
- Intended Use
- This product is used with "Meijia" automatic biochemical analyzer to quantitatively detect creatinine in human serum and plasma.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1225 Creatinine Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 08, 2014
- Expiry Date
- Apr 08, 2024
About this record
Access comprehensive regulatory information for “Medica” Creatinine Reagent Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e411d323221d38b6fe9d8a2206193415 and manufactured by MEDICA CORPORATION. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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