"Fujifilm" electronic digestive endoscope - Taiwan Registration 91b95133d00614785b399a8e8073c34a
Access comprehensive regulatory information for "Fujifilm" electronic digestive endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 91b95133d00614785b399a8e8073c34a and manufactured by FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION, 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
"Fujifilm" electronic digestive endoscope and its accessories
FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION
14254bf5fc44caa16d90568ae6d8431e
2
"Fujifilm" electronic digestive endoscope
FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION
151197decc3c91243686353204467868
2

