Taiwan FDA registration a9c916a8c3d22829cec8b718b4ebd765
"Bayerdenik" Sillo implantable heart rhythm regulator
TW: “拜耳德尼克”璽洛植入式心律調節器
Taiwan·Risk Class 3·BIOTRONIC SE & CO. KG·Registered Mar 09, 2007 – Mar 09, 2012CancelledRegistration details
- Analysis ID
- a9c916a8c3d22829cec8b718b4ebd765
- Customs Code
- DHA00601778409
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
- Mar 09, 2007
- Expiry Date
- Mar 09, 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 "Bayerdenik" Sillo implantable 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 a9c916a8c3d22829cec8b718b4ebd765 and manufactured by BIOTRONIC SE & CO. KG. The authorized representative in Taiwan is PRO PHARMA TAIWAN INC..
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