and light tube fluid - Taiwan Registration 8f450f51ca02767b1f6dbc2a4dfafb8f
Access comprehensive regulatory information for and light tube fluid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8f450f51ca02767b1f6dbc2a4dfafb8f and manufactured by FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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Device Details
Product Details
As a quality control serum for IgG, IgA, IgM, C3, C4, CRP, RF and ASO reagents.
A Clinical chemistry and clinical toxicology
A.1660 Quality control materials (analytical and non-analytical)
import
Dates and Status
Dec 15, 2005
Dec 15, 2025