Pure Global

"Dula Fox" coronary vascular stent system - Taiwan Registration d3a40c8312aa1c013e703ae38f5ce11e

Access comprehensive regulatory information for "Dula Fox" coronary vascular stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d3a40c8312aa1c013e703ae38f5ce11e and manufactured by GOODMAN MEDICAL IRELAND. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..

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
d3a40c8312aa1c013e703ae38f5ce11e
Registration Details
Taiwan FDA Registration: d3a40c8312aa1c013e703ae38f5ce11e
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Dula Fox" coronary vascular stent system
TW: โ€œๆœๆ‹‰ไฝ›ๅ…‹ๆ–ฏโ€ๅ† ็‹€ๅ‹•่„ˆ่ก€็ฎกๆ”ฏๆžถ็ณป็ตฑ
Risk Class 3
Cancelled

Registration Details

d3a40c8312aa1c013e703ae38f5ce11e

DHA00602285003

Company Information

Ireland

Product Details

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

E Cardiovascular Medicine Science

E.0001 Cardiovascular stents

import

Dates and Status

Oct 19, 2011

Oct 19, 2016

May 17, 2018

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ