Taiwan FDA registration 48c3dde49a227ab7afd32c4d47720163
“BIOTRONIK” Dynamic Peripheral Stent and Delivery System
TW: “百多力”黛納米周邊支架及輸送系統
Taiwan·Risk Class 2·MD·BIOTRONIK AG·Registered Apr 18, 2017 – Apr 18, 2027ActiveRegistration details
- Analysis ID
- 48c3dde49a227ab7afd32c4d47720163
- License Form
- Ministry of Health Medical Device Import No. 029664
- Customs Code
- DHA05602966408
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 devices
- Product Type (Level 2)
- E0001 Cardiovascular stents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 18, 2017
- Expiry Date
- Apr 18, 2027
About this record
Access comprehensive regulatory information for “BIOTRONIK” Dynamic Peripheral Stent and Delivery System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 48c3dde49a227ab7afd32c4d47720163 and manufactured by BIOTRONIK AG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.
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