Taiwan FDA registration 3b11509b0b896a7adfd85d4c4187bc76
“BIOTRONIK” Pulsar-18 Self Expanding Peripheral Stent System
TW: “百多力”帕撒18自行擴張周邊支架系統
Taiwan·Risk Class 2·MD·BIOTRONIK AG·Registered Sep 01, 2014 – Sep 01, 2024ExpiredRegistration details
- Analysis ID
- 3b11509b0b896a7adfd85d4c4187bc76
- License Form
- Ministry of Health Medical Device Import No. 026458
- Customs Code
- DHA05602645803
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
- Sep 01, 2014
- Expiry Date
- Sep 01, 2024
About this record
Access comprehensive regulatory information for “BIOTRONIK” Pulsar-18 Self Expanding Peripheral Stent System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3b11509b0b896a7adfd85d4c4187bc76 and manufactured by BIOTRONIK AG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.
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