Taiwan FDA registration 1fc72a9127dd3bc3200cc78965fe01a1

Fujifilm Digital Mammogram Imaging System

TW: 富士數位乳房X光影像系統
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Corporation;; FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office·Registered Jun 24, 2014 – Jun 24, 2029Active
Registration details
Analysis ID
1fc72a9127dd3bc3200cc78965fe01a1
Customs Code
DHAS5602636708
Company information
Manufacturer Country
Japan
Authorized Representative
FUJIFILM HEALTHCARE TAIWAN CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1710 乳房X光系統
Import Information
Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
Dates and status
Registration Date
Jun 24, 2014
Expiry Date
Jun 24, 2029
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About this record

Access comprehensive regulatory information for Fujifilm Digital Mammogram Imaging System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1fc72a9127dd3bc3200cc78965fe01a1 and manufactured by FUJIFILM Corporation;; FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. 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 TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE, 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.

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