Taiwan FDA registration 0b1ae39e39c4bfc8715a2f1f12a01f26
“MFM” Multilayer Flow Modulator Peripheral Stent System
TW: “漫孚渼” 多層血流調節周邊支架系統
Taiwan·Risk Class 3·MD·Cardiatis SA·Registered Feb 22, 2021 – Feb 22, 2026ExpiredRegistration details
- Analysis ID
- 0b1ae39e39c4bfc8715a2f1f12a01f26
- License Form
- Ministry of Health Medical Device Import No. 034038
- Customs Code
- DHA05603403803
Company information
- Manufacturer
- Cardiatis SA
- Manufacturer Country
- Belgium
- Authorized Representative
- GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E0006 Endovascular Transplantation System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 22, 2021
- Expiry Date
- Feb 22, 2026
About this record
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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