Taiwan FDA registration 34145e23084b14b2bff38cd169f6ebc1
“BIOTRONIK” Pantera Pro Coronary Dilatation Catheter
TW: “百多力” 帕得拉普羅冠狀動脈擴張導管
Taiwan·Risk Class 2·MD·BIOTRONIK AG·Registered Aug 16, 2016 – Aug 16, 2026ActiveRegistration details
- Analysis ID
- 34145e23084b14b2bff38cd169f6ebc1
- License Form
- Ministry of Health Medical Device Import No. 028767
- Customs Code
- DHA05602876700
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)
- E0005 Percutaneous puncture of the coronary ductus
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 16, 2016
- Expiry Date
- Aug 16, 2026
About this record
Access comprehensive regulatory information for “BIOTRONIK” Pantera Pro Coronary Dilatation Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 34145e23084b14b2bff38cd169f6ebc1 and manufactured by BIOTRONIK AG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices