Taiwan FDA registration bf79cfc2d04840d3054904468b5e04f5
"Caudix" Durising coronary artery dilation duct
TW: “考迪斯” 杜芮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
- bf79cfc2d04840d3054904468b5e04f5
- Customs Code
- DHA00601914409
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" Durising coronary artery dilation duct in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number bf79cfc2d04840d3054904468b5e04f5 and manufactured by CORDIS CASHEL. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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