Taiwan FDA registration c8e13ac8191bcee1758f3dc5469d276c

Fujifilm digital mammography system

TW: “富士” 數位乳房X光影像系統

Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION·Registered Sep 19, 2024 – Sep 19, 2029Active

Registration details

Analysis ID: c8e13ac8191bcee1758f3dc5469d276c
Customs Code: DHAS5603740807

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: Details are as detailed as approved Chinese instructions
Product Type (Level 1): P Radiology Science
Product Type (Level 2): P.1710 乳房X光系統
Import Information: The consent of the Nuclear Safety Commission must be obtained for each import of this medical device.;; input

Dates and status

Registration Date: Sep 19, 2024
Expiry Date: Sep 19, 2029

About this record

Access comprehensive regulatory information for Fujifilm digital mammography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c8e13ac8191bcee1758f3dc5469d276c 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.