Fujifilm endoscopy auxiliary interpretation software - Taiwan Registration 326590fb56d20084c396b297e761cdf0
Access comprehensive regulatory information for Fujifilm endoscopy auxiliary interpretation software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 326590fb56d20084c396b297e761cdf0 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN 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.
Device Details
Product Details
This product can detect and interpret areas suspected of large intestine polyps in the image output by the endoscope host.
H Gastroenterology and urology
H.9999 Miscellaneous
import
Dates and Status
Dec 15, 2022
Dec 15, 2027