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“BIOTRONIK” Dynamic Peripheral Stent and Delivery System - Taiwan Registration 48c3dde49a227ab7afd32c4d47720163

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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48c3dde49a227ab7afd32c4d47720163
Registration Details
Taiwan FDA Registration: 48c3dde49a227ab7afd32c4d47720163
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Device Details

“BIOTRONIK” Dynamic Peripheral Stent and Delivery System
TW: “百多力”黛納米周邊支架及輸送系統
Risk Class 2
MD

Registration Details

48c3dde49a227ab7afd32c4d47720163

Ministry of Health Medical Device Import No. 029664

DHA05602966408

Company Information

Switzerland

Product Details

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

E Cardiovascular devices

E0001 Cardiovascular stents

Imported from abroad

Dates and Status

Apr 18, 2017

Apr 18, 2027