Taiwan FDA registration 3d3ce67ef16a0fd9e43985f4afc3eadd
"Byrdnik" quick exchange coronary stent system
TW: “拜爾德尼克”快速交換冠狀動脈支架系統
Taiwan·Risk Class 3·BIOTRONIK AG·Registered May 09, 2008 – May 09, 2013CancelledRegistration details
- Analysis ID
- 3d3ce67ef16a0fd9e43985f4afc3eadd
- Customs Code
- DHA00601884903
Company information
- Manufacturer
- BIOTRONIK AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- PRO PHARMA TAIWAN INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.0001 Cardiovascular stents
- Import Information
- import
Dates and status
- Registration Date
- May 09, 2008
- Expiry Date
- May 09, 2013
- Cancellation Date
- Jun 17, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Byrdnik" quick exchange coronary stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3d3ce67ef16a0fd9e43985f4afc3eadd and manufactured by BIOTRONIK AG. The authorized representative in Taiwan is PRO PHARMA TAIWAN INC..
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