"Fujifilm" Blood Ammonia Quality Control Solution (Unsterilized) - Taiwan Registration bc5e6024e9a3c2566e83908145792906
Access comprehensive regulatory information for "Fujifilm" Blood Ammonia Quality Control 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 bc5e6024e9a3c2566e83908145792906 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..
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 of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
A Clinical chemistry and clinical toxicology
A.1660 Quality control materials (analytical and non-analytical)
Input;; QMS/QSD
Dates and Status
Sep 14, 2011
Sep 14, 2026