"DFI" Vaginal Discharge PH Rapid Test (Non-Sterile) - Taiwan Registration 793dd84a2b85c308df5dfb9c21099aae
Access comprehensive regulatory information for "DFI" Vaginal Discharge PH Rapid 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 793dd84a2b85c308df5dfb9c21099aae and manufactured by DFI CO.,LTD. The authorized representative in Taiwan is GORED ENTERPRISE CO., LTD..
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Device Details
Registration Details
793dd84a2b85c308df5dfb9c21099aae
Ministry of Health Medical Device Import No. 018012
DHA09401801200
Product Details
Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Uric pH (Non-quantitative) Test System (A.1550)".
A Clinical chemistry and clinical toxicology
A1550 Uric pH (non-quantitative) test system
Imported from abroad
Dates and Status
Jun 26, 2017
Jun 26, 2027