Taiwan FDA registration 14d130398710a18e986c1de5e14b3e9e
"Telmao" Ruilei second-generation thoracic aortic stent and delivery system
TW: “泰爾茂”瑞磊第二代胸主動脈覆膜支架暨輸送系統
Taiwan·Risk Class 3·BOLTON MEDICAL, INC.·Registered Nov 11, 2020 – Nov 11, 2025ExpiredRegistration details
- Analysis ID
- 14d130398710a18e986c1de5e14b3e9e
- Customs Code
- DHA05603408104
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
- Nov 11, 2020
- Expiry Date
- Nov 11, 2025
About this record
Access comprehensive regulatory information for "Telmao" Ruilei second-generation thoracic aortic stent and delivery system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 14d130398710a18e986c1de5e14b3e9e and manufactured by BOLTON MEDICAL, INC.. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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