Taiwan FDA registration 87e7d0a7496790c1e7eb59f237ce9dbe
"Medtronic" vascular catheter
TW: "美敦力"血管導管
Taiwan·Risk Class 2·MEDTRONIC NEUROMODULATION·Registered Aug 04, 2005 – Aug 04, 2015CancelledRegistration details
- Analysis ID
- 87e7d0a7496790c1e7eb59f237ce9dbe
- Customs Code
- DHA00601165405
Company information
- Manufacturer
- MEDTRONIC NEUROMODULATION
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5970 Percutaneous long-term implantable endovascular catheters
- Import Information
- import
Dates and status
- Registration Date
- Aug 04, 2005
- Expiry Date
- Aug 04, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Medtronic" vascular catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 87e7d0a7496790c1e7eb59f237ce9dbe and manufactured by MEDTRONIC NEUROMODULATION. 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