Taiwan FDA registration a88e8561bafb846cb22ff581ba20f348
"Shino-Test" Iron (non-heme) test (Non-Sterile)
TW: "錫諾" 鐵(非血基質)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
- a88e8561bafb846cb22ff581ba20f348
- License Form
- Ministry of Health Medical Device Import No. 014726
- Customs Code
- DHA09401472606
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Iron (Non-blood Matrix) Test System (A.1410)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1410 Iron (non-blood matrix) 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" Iron (non-heme) 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 a88e8561bafb846cb22ff581ba20f348 and manufactured by SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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