"DFI" Uric Acid Reagent (Non-Sterile) - Taiwan Registration 51e04b67fcba73faebed4633a7cb3140
Access comprehensive regulatory information for "DFI" Uric Acid Reagent (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 51e04b67fcba73faebed4633a7cb3140 and manufactured by DFI CO.,LTD. The authorized representative in Taiwan is GORED ENTERPRISE CO., LTD..
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Device Details
Registration Details
51e04b67fcba73faebed4633a7cb3140
Ministry of Health Medical Device Import No. 018011
DHA09401801101
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
Jun 26, 2017
Jun 26, 2022