Taiwan FDA registration adbf88d55b8eefa12a74059448ca54d2
"Medtronic" Vidor implantable cardiac defibrillator
TW: “美敦力”維多植入式心臟去顫器
Taiwan·Risk Class 3·MEDTRONIC EUROPE SARL·Registered Nov 29, 2007 – Nov 29, 2017CancelledRegistration details
- Analysis ID
- adbf88d55b8eefa12a74059448ca54d2
- Customs Code
- DHA00601846804
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
- Nov 29, 2007
- Expiry Date
- Nov 29, 2017
- 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 "Medtronic" Vidor 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 adbf88d55b8eefa12a74059448ca54d2 and manufactured by MEDTRONIC EUROPE SARL. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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