Pure Global

"Intec" Skobar peripheral vascular stent system - Taiwan Registration 4be8cf039c41034d5c553482ff617e97

Access comprehensive regulatory information for "Intec" Skobar peripheral 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 4be8cf039c41034d5c553482ff617e97 and manufactured by INVATEC S.P.A.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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
4be8cf039c41034d5c553482ff617e97
Registration Details
Taiwan FDA Registration: 4be8cf039c41034d5c553482ff617e97
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Intec" Skobar peripheral vascular stent system
TW: โ€œ่‹ฑๆณฐๅ…‹โ€ๆ–ฏๅฏๅทดๅ‘จ้‚Š่ก€็ฎกๆ”ฏๆžถ็ณป็ตฑ
Risk Class 3
Cancelled

Registration Details

4be8cf039c41034d5c553482ff617e97

DHA00602085707

Company Information

Italy

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

Mar 24, 2010

Mar 24, 2015

Apr 25, 2018

Cancellation Information

Logged out

่‡ช่กŒ้ตๅ…ฅ