Taiwan FDA registration 754fe810d116d540cd0ab5c388bec9f9
"Medtronic" Acetronia magnetic resonance implantable cardiac rhythmometer
TW: “美敦力”安信諾磁振造影植入式心臟節律器
Taiwan·Risk Class 3·Medtronic Inc.; Medtronic Europe Sàrl·Registered Jan 03, 2013 – Jan 03, 2028ActiveRegistration details
- Analysis ID
- 754fe810d116d540cd0ab5c388bec9f9
- Customs Code
- DHA00602438206
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
- Jan 03, 2013
- Expiry Date
- Jan 03, 2028
About this record
Access comprehensive regulatory information for "Medtronic" Acetronia magnetic resonance implantable cardiac rhythmometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 754fe810d116d540cd0ab5c388bec9f9 and manufactured by Medtronic Inc.; Medtronic Europe Sàrl. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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