Pure Global

“Hexacath” Peripheral Vascular Stent HELIOS SD Ti - Taiwan Registration 1630076e79ac51562a3631e3ad07ff76

Access comprehensive regulatory information for “Hexacath” Peripheral Vascular Stent HELIOS SD Ti in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1630076e79ac51562a3631e3ad07ff76 and manufactured by HEXACATH. The authorized representative in Taiwan is CATHERINE CONSULTANTS 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
1630076e79ac51562a3631e3ad07ff76
Registration Details
Taiwan FDA Registration: 1630076e79ac51562a3631e3ad07ff76
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Hexacath” Peripheral Vascular Stent HELIOS SD Ti
TW: “海斯凱”哈里歐-鈦周邊血管支架
Risk Class 2
MD

Registration Details

1630076e79ac51562a3631e3ad07ff76

Ministry of Health Medical Device Import No. 027428

DHA05602742802

Company Information

France

Product Details

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

E Cardiovascular devices

E0001 Cardiovascular stents

Imported from abroad

Dates and Status

Jun 17, 2015

Jun 17, 2025