Taiwan FDA registration 04e02fe83b5d1f0ee8df7a875f44ff30
“Medica” Blood Urea Nitrogen Reagent Kit (BUN)
TW: “美麗佳” 血尿素氮試劑
Taiwan·Risk Class 2·MD·MEDICA CORPORATION·Registered Jan 27, 2014 – Jan 27, 2024ExpiredRegistration details
- Analysis ID
- 04e02fe83b5d1f0ee8df7a875f44ff30
- License Form
- Ministry of Health Medical Device Import No. 025870
- Customs Code
- DHA05602587004
Company information
- Manufacturer
- MEDICA CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- GRAND MARQUIS CO., LTD.
Product details
- Intended Use
- This product is used in "Mirijia" automatic biochemical analyzer to quantitatively detect blood urea nitrogen in human serum and plasma.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1770 Urea nitrogen test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 27, 2014
- Expiry Date
- Jan 27, 2024
About this record
Access comprehensive regulatory information for “Medica” Blood Urea Nitrogen Reagent Kit (BUN) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 04e02fe83b5d1f0ee8df7a875f44ff30 and manufactured by MEDICA CORPORATION. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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