Taiwan FDA registration de37e60eeb6941ecfc8da7e96a383275
“Medica” Alkaline Phosphatase Reagent Kit (ALP)
TW: “美麗佳” 鹼性磷酸酶試劑
Taiwan·Risk Class 2·MD·MEDICA CORPORATION·Registered Jan 27, 2014 – Jan 27, 2024ExpiredRegistration details
- Analysis ID
- de37e60eeb6941ecfc8da7e96a383275
- License Form
- Ministry of Health Medical Device Import No. 025867
- Customs Code
- DHA05602586702
Company information
- Manufacturer
- MEDICA CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- GRAND MARQUIS CO., LTD.
Product details
- Intended Use
- This product is used in the "Mirijia" automatic biochemical analyzer to quantitatively detect alkaline phosphatase in human serum.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1050 Basic phosphoric acid? or isomeric feeding 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” Alkaline Phosphatase Reagent Kit (ALP) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number de37e60eeb6941ecfc8da7e96a383275 and manufactured by MEDICA CORPORATION. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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