Taiwan FDA registration 4a8aaa2ba92087354411f2730ef40e13
"Medtronic" Conset implantable cardiac defibrillator
TW: “美敦力”康賽特植入式心臟去顫器
Taiwan·Risk Class 3·MEDTRONIC EUROPE SARL·Registered Jul 30, 2009 – Jul 30, 2019CancelledRegistration details
- Analysis ID
- 4a8aaa2ba92087354411f2730ef40e13
- Customs Code
- DHA00602008404
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
- Jul 30, 2009
- Expiry Date
- Jul 30, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Medtronic" Conset implantable cardiac defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 4a8aaa2ba92087354411f2730ef40e13 and manufactured by MEDTRONIC EUROPE SARL. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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