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"Telmao" Ruilei second-generation thoracic aortic stent and delivery system - Taiwan Registration 14d130398710a18e986c1de5e14b3e9e

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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14d130398710a18e986c1de5e14b3e9e
Registration Details
Taiwan FDA Registration: 14d130398710a18e986c1de5e14b3e9e
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Device Details

"Telmao" Ruilei second-generation thoracic aortic stent and delivery system
TW: โ€œๆณฐ็ˆพ่Œ‚โ€็‘ž็ฃŠ็ฌฌไบŒไปฃ่ƒธไธปๅ‹•่„ˆ่ฆ†่†œๆ”ฏๆžถๆšจ่ผธ้€็ณป็ตฑ
Risk Class 3

Registration Details

14d130398710a18e986c1de5e14b3e9e

DHA05603408104

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.0006.

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

Nov 11, 2020

Nov 11, 2025