Taiwan FDA registration d4126020f40a2ca4ff1c4f40fede139c

Fujifilm Digital Mammogram Imaging System

TW: 富士數位乳房X光影像系統
Taiwan flagTaiwan·Risk Class 2·FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE·Registered Mar 20, 2013 – Mar 20, 2018Cancelled
Registration details
Analysis ID
d4126020f40a2ca4ff1c4f40fede139c
Customs Code
DHAS0602451201
Company information
Manufacturer Country
Japan
Authorized Representative
NAN KAI CORPORATION
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
Mar 20, 2013
Expiry Date
Mar 20, 2018
Cancellation Date
Dec 13, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 d4126020f40a2ca4ff1c4f40fede139c and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is NAN KAI CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE, FUJIFILM Corporation;; FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office, 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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