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"Decant Flex" aortic stent system - Taiwan Registration 4c2567de5b42705c1716b107e6c80d5f

Access comprehensive regulatory information for "Decant Flex" 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 4c2567de5b42705c1716b107e6c80d5f and manufactured by Bentley InnoMed GmbH. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.

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4c2567de5b42705c1716b107e6c80d5f
Registration Details
Taiwan FDA Registration: 4c2567de5b42705c1716b107e6c80d5f
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Device Details

"Decant Flex" aortic stent system
TW: โ€œๆฝท่‘›็ฟๅญšโ€ไธปๅ‹•่„ˆ่ฆ†่†œๆ”ฏๆžถ็ณป็ตฑ
Risk Class 3

Registration Details

4c2567de5b42705c1716b107e6c80d5f

DHA05603325200

Company Information

Germany

Product Details

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

E Cardiovascular Medicine Science

E.0006.

import

Dates and Status

Feb 12, 2020

Feb 12, 2030