Taiwan FDA registration 3141696a374b29ad908cc74ec8df1e83
"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 2·MEDTRONIC EUROPE SARL·Registered Apr 29, 2011 – Apr 29, 2021CancelledRegistration details
- Analysis ID
- 3141696a374b29ad908cc74ec8df1e83
- Customs Code
- DHA00602229402
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
- The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input
Dates and status
- Registration Date
- Apr 29, 2011
- Expiry Date
- Apr 29, 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 2 medical device is registered under number 3141696a374b29ad908cc74ec8df1e83 and manufactured by MEDTRONIC EUROPE SARL. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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