Taiwan FDA registration d933efce86cd1f9e7a44183c51eb4b4c
"Termao" Chuyou abdominal aortic stent system
TW: “泰爾茂”楚優腹主動脈支架系統
Taiwan·Risk Class 3·BOLTON MEDICAL, INC.·Registered Jul 27, 2020 – Jul 27, 2025ExpiredRegistration details
- Analysis ID
- d933efce86cd1f9e7a44183c51eb4b4c
- Customs Code
- DHA05603386102
Company information
- Manufacturer
- BOLTON MEDICAL, INC.
- Manufacturer Country
- United States
- 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.0006.
- Import Information
- The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input
Dates and status
- Registration Date
- Jul 27, 2020
- Expiry Date
- Jul 27, 2025
About this record
Access comprehensive regulatory information for "Termao" Chuyou abdominal aortic 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 d933efce86cd1f9e7a44183c51eb4b4c and manufactured by BOLTON MEDICAL, INC.. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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