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“AtriCure” AtriClip FLEX LAA Exclusion System - Taiwan Registration 40cff0ab0beeee78c60452fa9762482e

Access comprehensive regulatory information for “AtriCure” AtriClip FLEX LAA Exclusion System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 40cff0ab0beeee78c60452fa9762482e and manufactured by Atricure, Inc.. The authorized representative in Taiwan is ASIA HEALTH CARE 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.

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40cff0ab0beeee78c60452fa9762482e
Registration Details
Taiwan FDA Registration: 40cff0ab0beeee78c60452fa9762482e
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Device Details

“AtriCure” AtriClip FLEX LAA Exclusion System
TW: “艾翠科” 弗列斯左心耳閉塞夾系統
Risk Class 2
MD

Registration Details

40cff0ab0beeee78c60452fa9762482e

Ministry of Health Medical Device Import No. 034757

DHA05603475709

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular devices

E9999 Other

Imported from abroad

Dates and Status

Jul 13, 2021

Jul 13, 2026