Taiwan FDA registration cd896acd41604a4573f8b17c3f91aab2
"Medtronic" Evera implantable cardiac rectifier defibrillator
TW: “美敦力”艾維拉植入式心臟整流去顫器
Taiwan·Risk Class 3·Medtronic Inc.; Medtronic Europe Sàrl·Registered Oct 14, 2013 – Oct 14, 2028ActiveRegistration details
- Analysis ID
- cd896acd41604a4573f8b17c3f91aab2
- Customs Code
- DHA05602543206
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
- Oct 14, 2013
- Expiry Date
- Oct 14, 2028
About this record
Access comprehensive regulatory information for "Medtronic" Evera 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 cd896acd41604a4573f8b17c3f91aab2 and manufactured by Medtronic Inc.; Medtronic Europe Sàrl. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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