Taiwan FDA registration 23c95703d2e3d2f2dabbf6eac228d52f
“Medtronic” Micra Transcatheter Leadless Pacemaker System
TW: “美敦力”脈克拉無導線節律系統
Taiwan·Risk Class 3·MD·MEDTRONIC IRELAND·Registered Jan 18, 2017 – Jan 18, 2027ActiveRegistration details
- Analysis ID
- 23c95703d2e3d2f2dabbf6eac228d52f
- License Form
- Ministry of Health Medical Device Import No. 029037
- Customs Code
- DHA05602903707
Company information
- Manufacturer
- MEDTRONIC IRELAND
- Manufacturer Country
- Ireland
- 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 devices
- Product Type (Level 2)
- E3610 Pulse generator for implantable heart rhythm apparatus
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 18, 2017
- Expiry Date
- Jan 18, 2027
About this record
Access comprehensive regulatory information for “Medtronic” Micra Transcatheter Leadless Pacemaker System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 23c95703d2e3d2f2dabbf6eac228d52f and manufactured by MEDTRONIC IRELAND. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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