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“FUJIFILM” Workstation AMULET Bellus Software - Taiwan Registration 53f2ead7552b37d29d9a90fd1d8fcc7b

Access comprehensive regulatory information for “FUJIFILM” Workstation AMULET Bellus Software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 53f2ead7552b37d29d9a90fd1d8fcc7b and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE. 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.

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53f2ead7552b37d29d9a90fd1d8fcc7b
Registration Details
Taiwan FDA Registration: 53f2ead7552b37d29d9a90fd1d8fcc7b
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Device Details

“FUJIFILM” Workstation AMULET Bellus Software
TW: “富士”乳房影像工作站軟體
Risk Class 2
MD
Cancelled

Registration Details

53f2ead7552b37d29d9a90fd1d8fcc7b

Ministry of Health Medical Device Import No. 027728

DHA05602772801

Product Details

P Devices for radiology

P2050 Medical Image Management and Processing System

Imported from abroad

Dates and Status

Sep 10, 2015

Sep 10, 2020

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者