Taiwan FDA registration e2c894082e9e58f96cc10576f45bc875
"Medtronic" Smartra implantable cardiac defibrillator
TW: “美敦力”思格拉植入式心臟去顫器
Taiwan·Risk Class 3·MEDTRONIC EUROPE SARL·Registered Jul 30, 2009 – Jul 30, 2019CancelledRegistration details
- Analysis ID
- e2c894082e9e58f96cc10576f45bc875
- Customs Code
- DHA00602008302
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" Smartra 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 e2c894082e9e58f96cc10576f45bc875 and manufactured by MEDTRONIC EUROPE SARL. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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