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“GE”Medical image communication device (Non-Sterile) - Taiwan Registration 7cbf890cea72b3b8c2882b0ac65af30b

Access comprehensive regulatory information for “GE”Medical image communication device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7cbf890cea72b3b8c2882b0ac65af30b 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, 1 companies making similar products including GE HEALTHCARE FINLAND OY, and 1 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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7cbf890cea72b3b8c2882b0ac65af30b
Registration Details
Taiwan FDA Registration: 7cbf890cea72b3b8c2882b0ac65af30b
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Device Details

“GE”Medical image communication device (Non-Sterile)
TW: “奇異”醫學影像傳輸裝置 (未滅菌)
Risk Class 1
MD

Registration Details

7cbf890cea72b3b8c2882b0ac65af30b

Ministry of Health Medical Device Import No. 013438

DHA09401343809

Company Information

France

Product Details

Limited to the first-level recognition range of medical image transmission devices (P.2020) of the Measures for the Administration of Medical Devices.

P Devices for radiology

P2020 Medical Image Transmission Device

Imported from abroad

Dates and Status

Sep 18, 2013

Sep 18, 2023

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