Taiwan FDA registration 6d2f92015cbbfa21c8392ca94c7e700b

and light urine microalbumin correction solution

TW: 和光尿液微量白蛋白校正液組

Taiwan·Risk Class 2·FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT·Registered Nov 14, 2007 – Nov 14, 2027Active

Registration details

Analysis ID: 6d2f92015cbbfa21c8392ca94c7e700b
Customs Code: DHA00601867407

Company information

Manufacturer: FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT
Manufacturer Country: Japan
Authorized Representative: MEDICARE PRODUCTS INC.

Product details

Intended Use: Test corrector for measuring the amount of albumin in urine.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1150 Calibrated Products
Import Information: import

Dates and status

Registration Date: Nov 14, 2007
Expiry Date: Nov 14, 2027

About this record

Access comprehensive regulatory information for and light urine microalbumin correction solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6d2f92015cbbfa21c8392ca94c7e700b and manufactured by FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..

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