Taiwan FDA registration eadd0384da4348fdbeb5e02ccffa49dc
"Caudix" Farr star coronary artery dilation catheter
TW: “考迪斯” 法爾星冠狀動脈擴張導管
Taiwan·Risk Class 3·CORDIS CASHEL·Registered Jul 31, 2008 – Jul 31, 2018CancelledRegistration details
- Analysis ID
- eadd0384da4348fdbeb5e02ccffa49dc
- Customs Code
- DHA00601914307
Company information
- Manufacturer
- CORDIS CASHEL
- Manufacturer Country
- Ireland
- Authorized Representative
- EMERGO TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.0005.
- Import Information
- import
Dates and status
- Registration Date
- Jul 31, 2008
- Expiry Date
- Jul 31, 2018
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Caudix" Farr star coronary artery dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number eadd0384da4348fdbeb5e02ccffa49dc and manufactured by CORDIS CASHEL. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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