Pure Global

"Atrien" Advanda V12 PTFE laminated bracket - Taiwan Registration 13b91f0dc6384bd2c2c266c1eb0e9c17

Access comprehensive regulatory information for "Atrien" Advanda V12 PTFE laminated bracket in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 13b91f0dc6384bd2c2c266c1eb0e9c17 and manufactured by Atrium Medical Corporation. The authorized representative in Taiwan is GETINGE GROUP TAIWAN 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
13b91f0dc6384bd2c2c266c1eb0e9c17
Registration Details
Taiwan FDA Registration: 13b91f0dc6384bd2c2c266c1eb0e9c17
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Atrien" Advanda V12 PTFE laminated bracket
TW: โ€œไบž็ฟ ๆฉโ€่‰พๅพทๅ‡ก้”V12่šๅ››ๆฐŸไน™็ƒฏ ่ฆ†่†œๆ”ฏๆžถ
Risk Class 3

Registration Details

13b91f0dc6384bd2c2c266c1eb0e9c17

DHA00602233704

Company Information

United States

Product Details

Details such as Chinese copy of the imitation order Efficiency change: Details such as the Chinese copy of the imitation of the approved version

E Cardiovascular Medicine Science

E.0001 Cardiovascular stents

Input;; Contract manufacturing

Dates and Status

Jun 09, 2011

Jun 09, 2026