Taiwan FDA registration b97a2e98d96e1c60c908be0d52a6e67f
Weitai coronary expansion network management
TW: 威泰冠動脈擴充網管
Taiwan·MEDTRONIC INTERVENTIONAL VASCULAR EUROPE·Registered Mar 07, 1997 – Mar 07, 2002CancelledRegistration details
- Analysis ID
- b97a2e98d96e1c60c908be0d52a6e67f
- Customs Code
- DHA00600817101
Company information
- Manufacturer
- MEDTRONIC INTERVENTIONAL VASCULAR EUROPE
- Manufacturer Country
- Netherlands
- Authorized Representative
- KINGSTONE PRODUCTS (TAIWAN) LTD.
Product details
- Intended Use
- vacuum
- Product Type (Level 1)
- 0300 Prosthetic function substitute
- Import Information
- import
Dates and status
- Registration Date
- Mar 07, 1997
- Expiry Date
- Mar 07, 2002
- Cancellation Date
- Nov 17, 2004
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Weitai coronary expansion network management in Taiwan's medical device market through Pure Global AI's free database. is registered under number b97a2e98d96e1c60c908be0d52a6e67f and manufactured by MEDTRONIC INTERVENTIONAL VASCULAR EUROPE. The authorized representative in Taiwan is KINGSTONE PRODUCTS (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