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Fujifilm Digital Mammogram Imaging System - Taiwan Registration d4126020f40a2ca4ff1c4f40fede139c

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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d4126020f40a2ca4ff1c4f40fede139c
Registration Details
Taiwan FDA Registration: d4126020f40a2ca4ff1c4f40fede139c
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Device Details

Fujifilm Digital Mammogram Imaging System
TW: ๅฏŒๅฃซๆ•ธไฝไนณๆˆฟXๅ…‰ๅฝฑๅƒ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

d4126020f40a2ca4ff1c4f40fede139c

DHAS0602451201

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

P Radiology Science

P.1710 ไนณๆˆฟXๅ…‰็ณป็ตฑ

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

Mar 20, 2013

Mar 20, 2018

Dec 13, 2019

Cancellation Information

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