Pure Global

"Bioden" intravascular catheter fixation device (sterilized/unsterilized) - Taiwan Registration 765e7295e03478c1d51b3e67bbf4255a

Access comprehensive regulatory information for "Bioden" intravascular catheter fixation device (sterilized/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 765e7295e03478c1d51b3e67bbf4255a and manufactured by BIODERM INC.. The authorized representative in Taiwan is HUILI MEDICAL EQUIPMENT LIMITED.

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
765e7295e03478c1d51b3e67bbf4255a
Registration Details
Taiwan FDA Registration: 765e7295e03478c1d51b3e67bbf4255a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Bioden" intravascular catheter fixation device (sterilized/unsterilized)
TW: "็™พๆญ็™ป" ่ก€็ฎกๅ…งๅฐŽ็ฎกๅ›บๅฎš่ฃ็ฝฎ (ๆป…่Œ/ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

765e7295e03478c1d51b3e67bbf4255a

DHA09401754201

Company Information

United States

Product Details

Limited to the first level recognition range of endovascular catheter fixation device (J.5210) of the Measures for the Administration of Medical Devices.

J General hospital and personal use equipment

J.5210 ่ก€็ฎกๅ…งๅฐŽ็ฎกๅ›บๅฎš่ฃ็ฝฎ

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Mar 01, 2017

Mar 01, 2022

Apr 12, 2024

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ