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“GE” Functional Imaging Processing and Review System - Taiwan Registration 50908569ebf3e5be6b54bcd4e5fc20d9

Access comprehensive regulatory information for “GE” Functional Imaging Processing and Review System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 50908569ebf3e5be6b54bcd4e5fc20d9 and manufactured by GE MEDICAL SYSTEMS ISRAEL-FUNCTIONAL IMAGING. 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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50908569ebf3e5be6b54bcd4e5fc20d9
Registration Details
Taiwan FDA Registration: 50908569ebf3e5be6b54bcd4e5fc20d9
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Device Details

“GE” Functional Imaging Processing and Review System
TW: “奇異”醫學圖像紀錄傳輸系統
Risk Class 2
MD

Registration Details

50908569ebf3e5be6b54bcd4e5fc20d9

Ministry of Health Medical Device Import No. 029951

DHA05602995101

Company Information

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

Jun 30, 2017

Jun 30, 2027