Taiwan FDA registration d3a40c8312aa1c013e703ae38f5ce11e
"Dula Fox" coronary vascular stent system
TW: “杜拉佛克斯”冠狀動脈血管支架系統
Taiwan·Risk Class 3·GOODMAN MEDICAL IRELAND·Registered Oct 19, 2011 – Oct 19, 2016CancelledRegistration details
- Analysis ID
- d3a40c8312aa1c013e703ae38f5ce11e
- Customs Code
- DHA00602285003
Company information
- Manufacturer
- GOODMAN MEDICAL IRELAND
- Manufacturer Country
- Ireland
- Authorized Representative
- LEIN YIH MEDICAL CO.
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.0001 Cardiovascular stents
- Import Information
- import
Dates and status
- Registration Date
- Oct 19, 2011
- Expiry Date
- Oct 19, 2016
- Cancellation Date
- May 17, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Dula Fox" coronary vascular stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d3a40c8312aa1c013e703ae38f5ce11e and manufactured by GOODMAN MEDICAL IRELAND. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..
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