Taiwan FDA registration 70a559eb826e2253814ac16e3aef73be
"Medtronic" Astrography, implantable cardiac rhythmometer
TW: “美敦力”亞士卓磁振造影植入式心臟節律器
Taiwan·Risk Class 3·Medtronic Inc.; Medtronic Europe Sàrl·Registered Dec 28, 2017 – Dec 28, 2027ActiveRegistration details
- Analysis ID
- 70a559eb826e2253814ac16e3aef73be
- Customs Code
- DHA05603063501
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
- Dec 28, 2017
- Expiry Date
- Dec 28, 2027
About this record
Access comprehensive regulatory information for "Medtronic" Astrography, 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 70a559eb826e2253814ac16e3aef73be and manufactured by Medtronic Inc.; Medtronic Europe Sàrl. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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