Pure Global

"Termao" Chuyou abdominal aortic stent system - Taiwan Registration d933efce86cd1f9e7a44183c51eb4b4c

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
89,000+ Devices
d933efce86cd1f9e7a44183c51eb4b4c
Registration Details
Taiwan FDA Registration: d933efce86cd1f9e7a44183c51eb4b4c
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Termao" Chuyou abdominal aortic stent system
TW: โ€œๆณฐ็ˆพ่Œ‚โ€ๆฅšๅ„ช่…นไธปๅ‹•่„ˆๆ”ฏๆžถ็ณป็ตฑ
Risk Class 3

Registration Details

d933efce86cd1f9e7a44183c51eb4b4c

DHA05603386102

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

Jul 27, 2020

Jul 27, 2025