“Nipro” Hemodiafilter Fineflux - Taiwan Registration 1910c6884d20efd2978ff2ee23049b74

Access comprehensive regulatory information for “Nipro” Hemodiafilter Fineflux in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1910c6884d20efd2978ff2ee23049b74 and manufactured by Nipro Corporation Odate Factory. The authorized representative in Taiwan is HUA CHIANG MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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.