Taiwan FDA registration 277398bde22f5570774dc5a1b4bd2205
"Medtronic" Evera MRI implantable cardiac rectifier defibrillator
TW: “美敦力”艾維拉磁振造影植入式心臟整流去顫器
Taiwan·Risk Class 3·Medtronic Inc.; Medtronic Europe Sàrl·Registered Mar 09, 2016 – Mar 09, 2026ExpiredRegistration details
- Analysis ID
- 277398bde22f5570774dc5a1b4bd2205
- Customs Code
- DHA05602825308
Company information
- Manufacturer
- Medtronic Inc.; Medtronic Europe Sàrl
- Manufacturer Country
- United States;;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
- Mar 09, 2016
- Expiry Date
- Mar 09, 2026
About this record
Access comprehensive regulatory information for "Medtronic" Evera MRI implantable cardiac rectifier defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 277398bde22f5570774dc5a1b4bd2205 and manufactured by Medtronic Inc.; Medtronic Europe Sàrl. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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