Taiwan FDA registration 9713653ca170af4c6204827980327158
“Medtronic” CoreValve EnVeo PRO Delivery Catheter and Loading System
TW: “美敦力”柯普經導管主動脈瓣膜輸送及裝載系統
Taiwan·Risk Class 3·MD·MEDTRONIC IRELAND·Registered Dec 03, 2020 – Dec 03, 2025ExpiredRegistration details
- Analysis ID
- 9713653ca170af4c6204827980327158
- License Form
- Ministry of Health Medical Device Import No. 034201
- Customs Code
- DHA05603420101
Company information
- Manufacturer
- MEDTRONIC IRELAND
- Manufacturer Country
- Ireland
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- Details such as Chinese change in the performance of the approved copy of the imitation order: details such as the approved Chinese manual (the original approved label, instruction manual or packaging on December 24, 109 will be withdrawn and invalidated).
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E3925 Heart valve replacement
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 03, 2020
- Expiry Date
- Dec 03, 2025
About this record
Access comprehensive regulatory information for “Medtronic” CoreValve EnVeo PRO Delivery Catheter and Loading System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 9713653ca170af4c6204827980327158 and manufactured by MEDTRONIC IRELAND. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices