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"Kingyard" Catheter Securement Device (Non-Sterile) - Taiwan Registration 710e70f831fb04879d4dfafb335b82ee

Access comprehensive regulatory information for "Kingyard" Catheter Securement Device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 710e70f831fb04879d4dfafb335b82ee and manufactured by KINGYARD TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is KINGYARD TECHNOLOGY 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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710e70f831fb04879d4dfafb335b82ee
Registration Details
Taiwan FDA Registration: 710e70f831fb04879d4dfafb335b82ee
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Device Details

"Kingyard" Catheter Securement Device (Non-Sterile)
TW: "ๆ˜†้ˆบ" ๅฐŽ็ฎกๅ›บๅฎš่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

710e70f831fb04879d4dfafb335b82ee

Ministry of Health Medical Device Manufacturing No. 009331

Company Information

Taiwan, Province of China

Product Details

Limited to the first level recognition range of endovascular catheter fixation device (J.5210) of the classification and grading management method of medical equipment.

J General hospital and personal use equipment

J5210 Endovascular catheter fixation device

Produced in Taiwan, China

Dates and Status

Sep 27, 2021

Sep 27, 2026