Taiwan FDA registration 91f019e64dd25a7471ee0eda4fcc8a15
"Diffuse" multilayer blood flow regulates the aortic stent system
TW: “漫孚渼”多層血流調節主動脈支架系統
Taiwan·Risk Class 3·Cardiatis Ltd·Registered Nov 05, 2020 – Nov 05, 2025ExpiredRegistration details
- Analysis ID
- 91f019e64dd25a7471ee0eda4fcc8a15
- Customs Code
- DHA05603403204
Company information
- Manufacturer
- Cardiatis Ltd
- 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 Medicine Science
- Product Type (Level 2)
- E.0001 Cardiovascular stents
- Import Information
- The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input
Dates and status
- Registration Date
- Nov 05, 2020
- Expiry Date
- Nov 05, 2025
About this record
Access comprehensive regulatory information for "Diffuse" multilayer blood flow regulates the aortic 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 91f019e64dd25a7471ee0eda4fcc8a15 and manufactured by Cardiatis Ltd. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.
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