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"GE" Definium XR120 Digital X-ray imaging system - Taiwan Registration 46930c9f1aeb643ee0651db02928ff0b

Access comprehensive regulatory information for "GE" Definium XR120 Digital X-ray imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 46930c9f1aeb643ee0651db02928ff0b and manufactured by Rayence Co., Ltd.. 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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46930c9f1aeb643ee0651db02928ff0b
Registration Details
Taiwan FDA Registration: 46930c9f1aeb643ee0651db02928ff0b
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Device Details

"GE" Definium XR120 Digital X-ray imaging system
TW: "ๅฅ‡็•ฐ"Xๅ…‰ๆ•ธไฝๅตๆชขๅ™จ
Risk Class 2
MD

Registration Details

46930c9f1aeb643ee0651db02928ff0b

Ministry of Health Medical Device Import No. 034764

DHA05603476406

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

P Devices for radiology

P1650 fluoroscopic X-ray image intensifier

Imported from abroad

Dates and Status

Jul 20, 2021

Jul 20, 2026