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"Bai Duoli" Dainami renal artery peripheral vascular stent system - Taiwan Registration 0866760a9466684f878e9416dee353ee

Access comprehensive regulatory information for "Bai Duoli" Dainami renal artery peripheral vascular 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 0866760a9466684f878e9416dee353ee and manufactured by BIOTRONIK AG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.

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0866760a9466684f878e9416dee353ee
Registration Details
Taiwan FDA Registration: 0866760a9466684f878e9416dee353ee
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Device Details

"Bai Duoli" Dainami renal artery peripheral vascular stent system
TW: โ€œ็™พๅคšๅŠ›โ€้ป›็ด็ฑณ่…Žๅ‹•่„ˆๅ‘จ้‚Š่ก€็ฎกๆ”ฏๆžถ็ณป็ตฑ
Risk Class 3

Registration Details

0866760a9466684f878e9416dee353ee

DHA05602969608

Company Information

Switzerland

Product Details

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

E Cardiovascular Medicine Science

E.0001 Cardiovascular stents

import

Dates and Status

May 10, 2017

May 10, 2027