Taiwan FDA registration 0866760a9466684f878e9416dee353ee
"Bai Duoli" Dainami renal artery peripheral vascular stent system
TW: “百多力”黛納米腎動脈周邊血管支架系統
Taiwan·Risk Class 3·BIOTRONIK AG·Registered May 10, 2017 – May 10, 2027ActiveRegistration details
- Analysis ID
- 0866760a9466684f878e9416dee353ee
- Customs Code
- DHA05602969608
Company information
- Manufacturer
- BIOTRONIK AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- BIOTRONIK TAIWAN LIMITED
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
- import
Dates and status
- Registration Date
- May 10, 2017
- Expiry Date
- May 10, 2027
About this record
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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