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“GE”Medical image communication device (Non-Sterile) - Taiwan Registration 78830ecb638cd520ade4cc0429d4a283

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 78830ecb638cd520ade4cc0429d4a283 and manufactured by GE HEALTHCARE FINLAND OY. 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 MEDICAL SYSTEMS S.C.S, 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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78830ecb638cd520ade4cc0429d4a283
Registration Details
Taiwan FDA Registration: 78830ecb638cd520ade4cc0429d4a283
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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

78830ecb638cd520ade4cc0429d4a283

Ministry of Health Medical Device Import No. 013571

DHA09401357101

Company Information

Finland

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

Nov 07, 2013

Nov 07, 2023

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