Taiwan FDA registration 37a36f9238d859e4bbaa449f4e9225a9
"Bayerdenick" PuraP quickly exchanges coronary balloon dilation catheters
TW: "拜耳德尼克"培力快速交換冠狀動脈氣球擴張術導管
Taiwan·Risk Class 3·BIOTRONIK AG·Registered Nov 24, 2006 – Nov 24, 2011CancelledRegistration details
- Analysis ID
- 37a36f9238d859e4bbaa449f4e9225a9
- Customs Code
- DHA00601745707
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
- Nov 24, 2006
- Expiry Date
- Nov 24, 2011
- Cancellation Date
- Oct 30, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bayerdenick" PuraP quickly exchanges coronary balloon dilation catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 37a36f9238d859e4bbaa449f4e9225a9 and manufactured by BIOTRONIK AG. The authorized representative in Taiwan is PRO PHARMA TAIWAN INC..
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