“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.
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Device Details
Registration Details
0b1ae39e39c4bfc8715a2f1f12a01f26
Ministry of Health Medical Device Import No. 034038
DHA05603403803
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

