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"Canon" Aplio i900/i800/i700 Diagnostic Ultrasound System - Taiwan Registration 8da55a0eca29c814d0bb2631a11ea82c

Access comprehensive regulatory information for "Canon" Aplio i900/i800/i700 Diagnostic Ultrasound System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8da55a0eca29c814d0bb2631a11ea82c and manufactured by Canon Medical Systems Corporation. 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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8da55a0eca29c814d0bb2631a11ea82c
Registration Details
Taiwan FDA Registration: 8da55a0eca29c814d0bb2631a11ea82c
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Device Details

"Canon" Aplio i900/i800/i700 Diagnostic Ultrasound System
TW: "ไฝณ่ƒฝ"่จบๆ–ท่ถ…้Ÿณๆณข็ณป็ตฑ
Risk Class 2
MD

Registration Details

8da55a0eca29c814d0bb2631a11ea82c

Ministry of Health Medical Device Import No. 030790

DHA05603079000

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

P Devices for radiology

P1550 ultrasonic pulsating Doppler imaging system

Imported from abroad

Dates and Status

Mar 29, 2018

Mar 29, 2028