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"Diffuse" multilayer blood flow regulates the aortic stent system - Taiwan Registration 91f019e64dd25a7471ee0eda4fcc8a15

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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91f019e64dd25a7471ee0eda4fcc8a15
Registration Details
Taiwan FDA Registration: 91f019e64dd25a7471ee0eda4fcc8a15
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Device Details

"Diffuse" multilayer blood flow regulates the aortic stent system
TW: โ€œๆผซๅญšๆธผโ€ๅคšๅฑค่ก€ๆต่ชฟ็ฏ€ไธปๅ‹•่„ˆๆ”ฏๆžถ็ณป็ตฑ
Risk Class 3

Registration Details

91f019e64dd25a7471ee0eda4fcc8a15

DHA05603403204

Company Information

Belgium

Product Details

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

E Cardiovascular Medicine Science

E.0001 Cardiovascular stents

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

Nov 05, 2020

Nov 05, 2025