Taiwan FDA registration cfef8f9a58e0f0b90816b1f3ce080404
“Medica” Creatine Kinase Reagent Kit
TW: “美麗佳” 肌酸激酶試劑
Taiwan·Risk Class 2·MD·MEDICA CORPORATION·Registered Apr 03, 2014 – Apr 03, 2024ExpiredRegistration details
- Analysis ID
- cfef8f9a58e0f0b90816b1f3ce080404
- License Form
- Ministry of Health Medical Device Import No. 025934
- Customs Code
- DHA05602593404
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 creatine kinase in human serum.
- 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 03, 2014
- Expiry Date
- Apr 03, 2024
About this record
Access comprehensive regulatory information for “Medica” Creatine Kinase 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 cfef8f9a58e0f0b90816b1f3ce080404 and manufactured by MEDICA CORPORATION. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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