Taiwan FDA registration f1ef34b00bf484c311e5d90086d2360e
"Shino-Test" Uric acid test (Non-Sterile)
TW: "錫諾" 尿酸檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER·Registered Dec 05, 2014 – Dec 05, 2024ExpiredRegistration details
- Analysis ID
- f1ef34b00bf484c311e5d90086d2360e
- License Form
- Ministry of Health Medical Device Import No. 014729
- Customs Code
- DHA09401472902
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- Limited to the first level identification range of the "uric acid test system (A.1775)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1775 Uric acid test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 05, 2014
- Expiry Date
- Dec 05, 2024
About this record
Access comprehensive regulatory information for "Shino-Test" Uric acid test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f1ef34b00bf484c311e5d90086d2360e and manufactured by SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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