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“GE” Medical Diagnostic Mammography Software System - Taiwan Registration 12d3e2febd72142e9e0d284c67611a82

Access comprehensive regulatory information for “GE” Medical Diagnostic Mammography Software System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 12d3e2febd72142e9e0d284c67611a82 and manufactured by GE MEDICAL SYSTEMS S.C.S. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, 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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12d3e2febd72142e9e0d284c67611a82
Registration Details
Taiwan FDA Registration: 12d3e2febd72142e9e0d284c67611a82
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Device Details

“GE” Medical Diagnostic Mammography Software System
TW: “奇異”乳房攝影軟體系統
Risk Class 2
MD

Registration Details

12d3e2febd72142e9e0d284c67611a82

Ministry of Health Medical Device Import No. 030151

DHA05603015105

Company Information

France

Product Details

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

P Devices for radiology

P2050 Medical Image Management and Processing System

Imported from abroad

Dates and Status

Aug 15, 2017

Aug 15, 2027