Taiwan FDA registration 4899c56bf67f659702d35381e8991582
"Bayerdenik" Setex implantable cardiac synchronization therapy heart rhythm regulator
TW: “拜耳德尼克”璽特司植入式心臟同步治療心律調節器
Taiwan·Risk Class 3·BIOTRONIC SE & CO. KG·Registered Oct 29, 2007 – Oct 29, 2017CancelledRegistration details
- Analysis ID
- 4899c56bf67f659702d35381e8991582
- Customs Code
- DHA00601837803
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.3610 Pulsator of implantable cardiac rhythm apparatus
- Import Information
- import
Dates and status
- Registration Date
- Oct 29, 2007
- Expiry Date
- Oct 29, 2017
- Cancellation Date
- Oct 25, 2013
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Bayerdenik" Setex implantable cardiac synchronization therapy heart rhythm regulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 4899c56bf67f659702d35381e8991582 and manufactured by BIOTRONIC SE & CO. KG. The authorized representative in Taiwan is PRO PHARMA TAIWAN INC..
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