Taiwan FDA registration 854c80f065c42e9f9a310a7288a179e8
Medtronic "Botdo Eti Implantable Cardiac Rectifier Defibrillator
TW: 美敦力”博特多艾緹植入式心臟整流去顫器
Taiwan·Risk Class 3·MEDTRONIC EUROPE SARL·Registered Jun 03, 2011 – Jun 03, 2021CancelledRegistration details
- Analysis ID
- 854c80f065c42e9f9a310a7288a179e8
- Customs Code
- DHA00602233105
Company information
- Manufacturer
- MEDTRONIC EUROPE SARL
- Manufacturer Country
- Switzerland
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
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
- Jun 03, 2011
- Expiry Date
- Jun 03, 2021
- Cancellation Date
- Sep 26, 2020
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Medtronic "Botdo Eti Implantable Cardiac Rectifier Defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 854c80f065c42e9f9a310a7288a179e8 and manufactured by MEDTRONIC EUROPE SARL. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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