Taiwan FDA registration bda1554e53fdc32342eac323f9b463d0
"Bayer Dennick" Kent intracardiac defibrillator lead
TW: “拜耳德尼克”肯特心內除顫器導線
Taiwan·Risk Class 3·BIOTRONIC SE & CO. KG·Registered Apr 10, 2007 – Apr 10, 2012CancelledRegistration details
- Analysis ID
- bda1554e53fdc32342eac323f9b463d0
- Customs Code
- DHA00601799509
Company information
- Manufacturer
- BIOTRONIC SE & CO. KG
- Manufacturer Country
- Germany
- 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.3680 心血管用永久或暫時性之心律調節器電極
- Import Information
- import
Dates and status
- Registration Date
- Apr 10, 2007
- Expiry Date
- Apr 10, 2012
- Cancellation Date
- May 05, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bayer Dennick" Kent intracardiac defibrillator lead in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number bda1554e53fdc32342eac323f9b463d0 and manufactured by BIOTRONIC SE & CO. KG. The authorized representative in Taiwan is PRO PHARMA TAIWAN INC..
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