Pure Global

“Taewoong” Pyloric/Duodenal Stent - Taiwan Registration 5672251ad4aa948a22eedb5bac8f43b5

Access comprehensive regulatory information for “Taewoong” Pyloric/Duodenal Stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5672251ad4aa948a22eedb5bac8f43b5 and manufactured by TAEWOONG MEDICAL CO., LTD.. The authorized representative in Taiwan is HOPE SING MEDICAL INSTRUMENTS 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
5672251ad4aa948a22eedb5bac8f43b5
Registration Details
Taiwan FDA Registration: 5672251ad4aa948a22eedb5bac8f43b5
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Taewoong” Pyloric/Duodenal Stent
TW: “泰悟”幽門/十二指腸支架
Risk Class 2
MD

Registration Details

5672251ad4aa948a22eedb5bac8f43b5

Ministry of Health Medical Device Import No. 031287

DHA05603128709

Company Information

Korea, Republic of

Product Details

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

I General and plastic surgical devices

I3610 Esophageal supplements

Imported from abroad

Dates and Status

Jul 06, 2018

Jul 06, 2028