"Hanyang" low ion buffer solution (unsterilized) - Taiwan Registration a5bc5fb8a1a2379cdf45e8fdbc89752a
Access comprehensive regulatory information for "Hanyang" low ion buffer solution (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a5bc5fb8a1a2379cdf45e8fdbc89752a and manufactured by METEK LAB INC.. The authorized representative in Taiwan is METEK LAB INC..
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.
Device Details
Product Details
Limited to the classification and grading management method of medical equipment, in vitro diagnostic intensive medium (B.9600) first level identification range.
B Hematology, pathology, and genetics
B.9600 Intensive medium for in vitro diagnostics
ๅ็ข;; QMS/QSD
Dates and Status
Aug 24, 2021
Aug 24, 2026

