Taiwan FDA registration 9e3e44199e46508ce075f4f132b8febe

and photoalkaline phosphatase reagent

TW: 和光鹼性磷酸酶試劑
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Wako Pure Chemical Corporation Mie Plant·Registered Sep 25, 2023 – Sep 25, 2028Active
Registration details
Analysis ID
9e3e44199e46508ce075f4f132b8febe
Customs Code
DHA05603622502
Company information
Manufacturer Country
Japan
Authorized Representative
MEDICARE PRODUCTS INC.
Product details
Intended Use
This product is used to quantitatively determine the activity of alkaline phosphatase (ALP) in serum or plasma.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1050 Alkaline phosphatase or isoenzyme testing system
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
Sep 25, 2023
Expiry Date
Sep 25, 2028
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About this record

Access comprehensive regulatory information for and photoalkaline phosphatase reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9e3e44199e46508ce075f4f132b8febe and manufactured by FUJIFILM Wako Pure Chemical Corporation Mie Plant. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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