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"Xinli" high-pressure contrast injection extension tube - Taiwan Registration 4a4f3cec1abf0f17e1f1dfaa76ba16e6

Access comprehensive regulatory information for "Xinli" high-pressure contrast injection extension tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4a4f3cec1abf0f17e1f1dfaa76ba16e6 and manufactured by SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD.. The authorized representative in Taiwan is CATHERINE CONSULTANTS 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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4a4f3cec1abf0f17e1f1dfaa76ba16e6
Registration Details
Taiwan FDA Registration: 4a4f3cec1abf0f17e1f1dfaa76ba16e6
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Device Details

"Xinli" high-pressure contrast injection extension tube
TW: โ€œๆ˜•ๅŠ›โ€้ซ˜ๅฃ“้€ ๅฝฑๆณจๅฐ„ๅปถ้•ท็ฎก
Risk Class 2

Registration Details

4a4f3cec1abf0f17e1f1dfaa76ba16e6

DHA09200081400

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.1650 ่ก€็ฎกๆ”ๅฝฑๆณจๅฐ„ๅ™จๅ’Œๆณจๅฐ„็ญ’

Input;; Chinese goods

Dates and Status

Feb 14, 2017

Feb 14, 2027