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Taiwan FDA registration 8f450f51ca02767b1f6dbc2a4dfafb8f

and light tube fluid

TW: 和光品管液
Taiwan flagTaiwan·Risk Class 2·FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT·Registered Dec 15, 2005 – Dec 15, 2025Expired
Registration details
Analysis ID
8f450f51ca02767b1f6dbc2a4dfafb8f
Customs Code
DHA00601559601
Company information
Manufacturer
FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT
Manufacturer Country
Japan
Authorized Representative
MEDICARE PRODUCTS INC.
Product details
Intended Use
As a quality control serum for IgG, IgA, IgM, C3, C4, CRP, RF and ASO reagents.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1660 Quality control materials (analytical and non-analytical)
Import Information
import
Dates and status
Registration Date
Dec 15, 2005
Expiry Date
Dec 15, 2025
About this record

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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