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“Canon” Digital Radiography CXDI-Pro - Taiwan Registration 4b5cd3a067cbe851387c33fd92021b83

Access comprehensive regulatory information for “Canon” Digital Radiography CXDI-Pro in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b5cd3a067cbe851387c33fd92021b83 and manufactured by CANON COMPONENTS, INC.. The authorized representative in Taiwan is ROTARY TRADING CO., 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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4b5cd3a067cbe851387c33fd92021b83
Registration Details
Taiwan FDA Registration: 4b5cd3a067cbe851387c33fd92021b83
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Device Details

“Canon” Digital Radiography CXDI-Pro
TW: “佳能” 數位放射攝影偵檢器
Risk Class 2
MD

Registration Details

4b5cd3a067cbe851387c33fd92021b83

Ministry of Health Medical Device Import No. 036377

DHA05603637709

Company Information

Japan

Product Details

Details are as detailed as approved Chinese instructions

P Radiology Science

P1650 fluoroscopic X-ray image intensifier

Imported from abroad

Dates and Status

Jun 10, 2023

Jun 10, 2028