Taiwan FDA registration 8d35665078e3730a683ecd91c5dbe550
"Termao" Jesft reinforced artificial blood vessels
TW: "泰爾茂"傑斯弗特加強型人工血管
Taiwan·Risk Class 2·VASCUTEK LTD.·Registered Aug 28, 2006 – Aug 28, 2026ActiveRegistration details
- Analysis ID
- 8d35665078e3730a683ecd91c5dbe550
- Customs Code
- DHA00601705401
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 28, 2006
- Expiry Date
- Aug 28, 2026
About this record
Access comprehensive regulatory information for "Termao" Jesft reinforced 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 8d35665078e3730a683ecd91c5dbe550 and manufactured by VASCUTEK LTD.. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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