"ARKRA" urinalysis tester (unsterilized) - Taiwan Registration 951471b6bf0cb1c7ac6052c4f09cbdda
Access comprehensive regulatory information for "ARKRA" urinalysis tester (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 951471b6bf0cb1c7ac6052c4f09cbdda and manufactured by Arkray Factory Inc., Head office factory. The authorized representative in Taiwan is SYNGEN BIOTECH CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ARKRAY INDUSTRY, INC., and 2 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.
Device Details
Product Details
Limited to the first level identification range of the "Automatic Urinalysis System (A.2900)" of the Measures for the Administration of Medical Devices.
A Clinical chemistry and clinical toxicology
A.2900 Automated urinalysis system
Dates and Status
Nov 17, 2006
Nov 17, 2026
Sep 30, 2021
Cancellation Information
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