Taiwan FDA registration 326590fb56d20084c396b297e761cdf0

Fujifilm endoscopy auxiliary interpretation software

TW: “富士”內視鏡檢查輔助判讀軟體

Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION·Registered Dec 15, 2022 – Dec 15, 2027Active

Registration details

Analysis ID: 326590fb56d20084c396b297e761cdf0
Customs Code: DHA05603594604

Company information

Manufacturer: FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION
Manufacturer Country: Japan
Authorized Representative: FUJIFILM HEALTHCARE TAIWAN CO., LTD.

Product details

Intended Use: This product can detect and interpret areas suspected of large intestine polyps in the image output by the endoscope host.
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.9999 Miscellaneous
Import Information: import

Dates and status

Registration Date: Dec 15, 2022
Expiry Date: Dec 15, 2027

About this record

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.