Taiwan FDA registration c1ca2dcae1056a1aa9b38818de406ec8
"Termao" Jesft artificial blood vessels
TW: "泰爾茂"傑斯弗特人工血管
Taiwan·Risk Class 2·VASCUTEK LTD.·Registered Aug 29, 2006 – Aug 29, 2021CancelledRegistration details
- Analysis ID
- c1ca2dcae1056a1aa9b38818de406ec8
- Customs Code
- DHA00601705500
Company information
- Manufacturer
- VASCUTEK LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
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.3450 血管移植彌補物
- Import Information
- import
Dates and status
- Registration Date
- Aug 29, 2006
- Expiry Date
- Aug 29, 2021
- Cancellation Date
- Oct 12, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Termao" Jesft artificial blood vessels in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c1ca2dcae1056a1aa9b38818de406ec8 and manufactured by VASCUTEK LTD.. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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