Taiwan FDA registration b40c456333ca276b3c469fcf30fff3ed
“Medtronic ” Complete SE Vascular Stent System
TW: “美敦力” 康博立血管自膨式支架系統
Taiwan·Risk Class 2·MD·MEDTRONIC IRELAND·Registered Mar 07, 2014 – Mar 07, 2019CancelledRegistration details
- Analysis ID
- b40c456333ca276b3c469fcf30fff3ed
- License Form
- Ministry of Health Medical Device Import No. 025831
- Customs Code
- DHA05602583107
Company information
- Manufacturer
- MEDTRONIC IRELAND
- Manufacturer Country
- Ireland
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E0001 Cardiovascular stents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 07, 2014
- Expiry Date
- Mar 07, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for “Medtronic ” Complete SE Vascular Stent System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b40c456333ca276b3c469fcf30fff3ed 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