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"Inofi" ureteral guide sheath - Taiwan Registration 3d6f64df0435d506c8f215d458b8d012

Access comprehensive regulatory information for "Inofi" ureteral guide sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3d6f64df0435d506c8f215d458b8d012 and manufactured by INNOVEX MEDICAL CO., LTD.. The authorized representative in Taiwan is INNOFUTURE INTERNATIONAL INC..

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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3d6f64df0435d506c8f215d458b8d012
Registration Details
Taiwan FDA Registration: 3d6f64df0435d506c8f215d458b8d012
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Device Details

"Inofi" ureteral guide sheath
TW: โ€œๅ› ่ซพๆ–โ€่ผธๅฐฟ็ฎกๅฐŽๅผ•้ž˜
Risk Class 2

Registration Details

3d6f64df0435d506c8f215d458b8d012

DHA09200115300

Company Information

China

Product Details

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

H Gastroenterology and urology

H.5130 ๆณŒๅฐฟๅฐŽ็ฎกๅŠๅ…ถ้™„ไปถ

Input;; Chinese goods

Dates and Status

Apr 01, 2020

Apr 01, 2025