Taiwan FDA registration 2e4b1e8e9bdc032d3ba25d5afb829742
Temporary Rhythm Apparatus "Medtronic"
TW: 暫時性節律器 〝美敦力〞
Taiwan·Risk Class 3·Medtronic Inc.·Registered Feb 06, 1998 – Feb 06, 2018CancelledRegistration details
- Analysis ID
- 2e4b1e8e9bdc032d3ba25d5afb829742
- Customs Code
- DHA00600854901
Company information
- Manufacturer
- Medtronic Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Product Type (Level 1)
- 0609 Extracorporeal cardiac plasticist
- Import Information
- import
Dates and status
- Registration Date
- Feb 06, 1998
- Expiry Date
- Feb 06, 2018
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Temporary Rhythm Apparatus "Medtronic" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2e4b1e8e9bdc032d3ba25d5afb829742 and manufactured by Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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