Pure Global

“MFM” Multilayer Flow Modulator Peripheral Stent System - Taiwan Registration 0b1ae39e39c4bfc8715a2f1f12a01f26

Access comprehensive regulatory information for “MFM” Multilayer Flow Modulator Peripheral 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 0b1ae39e39c4bfc8715a2f1f12a01f26 and manufactured by Cardiatis SA. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.

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
0b1ae39e39c4bfc8715a2f1f12a01f26
Registration Details
Taiwan FDA Registration: 0b1ae39e39c4bfc8715a2f1f12a01f26
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“MFM” Multilayer Flow Modulator Peripheral Stent System
TW: “漫孚渼” 多層血流調節周邊支架系統
Risk Class 3
MD

Registration Details

0b1ae39e39c4bfc8715a2f1f12a01f26

Ministry of Health Medical Device Import No. 034038

DHA05603403803

Company Information

Belgium

Product Details

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

E Cardiovascular devices

E0006 Endovascular Transplantation System

Imported from abroad

Dates and Status

Feb 22, 2021

Feb 22, 2026