"Arkra" ammonia analyzer (unsterilized) - Taiwan Registration 9a2e67dc94076da8a6a861abce5773f9
Access comprehensive regulatory information for "Arkra" ammonia analyzer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9a2e67dc94076da8a6a861abce5773f9 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 Factory Inc., Head office factory, 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.
Device Details
Product Details
Limited to the first level identification range of the blood ammonia test system (A.1065) of the management method for medical equipment.
A Clinical chemistry and clinical toxicology
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import
Dates and Status
Aug 05, 2010
Aug 05, 2020
Jul 15, 2022
Cancellation Information
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