"Fujifilm" electronic duodenoscopy - Taiwan Registration 42c2a61b358410e74d9ad895b721a054

Access comprehensive regulatory information for "Fujifilm" electronic duodenoscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 42c2a61b358410e74d9ad895b721a054 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 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.