"Shino-Test" Uric acid test (Non-Sterile) - Taiwan Registration f1ef34b00bf484c311e5d90086d2360e
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..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Registration Details
f1ef34b00bf484c311e5d90086d2360e
Ministry of Health Medical Device Import No. 014729
DHA09401472902
Product Details
Limited to the first level identification range of the "uric acid test system (A.1775)" of the Measures for the Administration of Medical Devices.
A Clinical chemistry and clinical toxicology
A1775 Uric acid test system
Imported from abroad
Dates and Status
Dec 05, 2014
Dec 05, 2024

