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“BIOTRONIK” Pantera Pro Coronary Dilatation Catheter - Taiwan Registration 34145e23084b14b2bff38cd169f6ebc1

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.

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34145e23084b14b2bff38cd169f6ebc1
Registration Details
Taiwan FDA Registration: 34145e23084b14b2bff38cd169f6ebc1
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Device Details

“BIOTRONIK” Pantera Pro Coronary Dilatation Catheter
TW: “百多力” 帕得拉普羅冠狀動脈擴張導管
Risk Class 2
MD

Registration Details

34145e23084b14b2bff38cd169f6ebc1

Ministry of Health Medical Device Import No. 028767

DHA05602876700

Company Information

Switzerland

Product Details

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

E Cardiovascular devices

E0005 Percutaneous puncture of the coronary ductus

Imported from abroad

Dates and Status

Aug 16, 2016

Aug 16, 2026