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"Aconn" Catheter Fixation Device (Sterilized) - Taiwan Registration 7c93730255a0aeeeabadd78eab8194c8

Access comprehensive regulatory information for "Aconn" Catheter Fixation Device (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7c93730255a0aeeeabadd78eab8194c8 and manufactured by ARGON MEDICAL DEVICES, INC.. The authorized representative in Taiwan is CHINA SPRING 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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7c93730255a0aeeeabadd78eab8194c8
Registration Details
Taiwan FDA Registration: 7c93730255a0aeeeabadd78eab8194c8
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Device Details

"Aconn" Catheter Fixation Device (Sterilized)
TW: โ€œไบžๅบทๆฉโ€ ๅฐŽ็ฎกๅ›บๅฎš่ฃ็ฝฎ (ๆป…่Œ)
Risk Class 1

Registration Details

7c93730255a0aeeeabadd78eab8194c8

DHA09402325000

Company Information

United States

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

J.5210 ่ก€็ฎกๅ…งๅฐŽ็ฎกๅ›บๅฎš่ฃ็ฝฎ

Input;; QMS/QSD

Dates and Status

Sep 21, 2023

Sep 21, 2028