Taiwan FDA registration 49596c37f21859063db2de5feca030d1

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 Apr 17, 2009 – Apr 17, 2024Expired
Registration details
Analysis ID
49596c37f21859063db2de5feca030d1
Customs Code
DHA00601999404
Company information
Manufacturer Country
Japan
Authorized Representative
MEDICARE PRODUCTS INC.
Product details
Intended Use
It 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
import
Dates and status
Registration Date
Apr 17, 2009
Expiry Date
Apr 17, 2024
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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 49596c37f21859063db2de5feca030d1 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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