Taiwan FDA registration 974d4d2a987d6af19b5697809a11aecb
"Medtronic" Avitha MRI implantable cardiac rhythmometer
TW: “美敦力”艾維莎磁振造影植入式心臟節律器
Taiwan·Risk Class 3·Medtronic Inc.; Medtronic Europe Sàrl·Registered Nov 25, 2011 – Nov 25, 2026ActiveRegistration details
- Analysis ID
- 974d4d2a987d6af19b5697809a11aecb
- Customs Code
- DHA00602311800
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
- Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.
Dates and status
- Registration Date
- Nov 25, 2011
- Expiry Date
- Nov 25, 2026
About this record
Access comprehensive regulatory information for "Medtronic" Avitha MRI 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 974d4d2a987d6af19b5697809a11aecb and manufactured by Medtronic Inc.; Medtronic Europe Sàrl. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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