Pure Global

“Edwards” Carpentier-Edwards PERIMOUNT Pericardial Bioprosthesis - Taiwan Registration f264893b9be6bc4354e66a892964cbc0

Access comprehensive regulatory information for “Edwards” Carpentier-Edwards PERIMOUNT Pericardial Bioprosthesis in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number f264893b9be6bc4354e66a892964cbc0 and manufactured by EDWARDS LIFESCIENCES LLC. The authorized representative in Taiwan is EDWARDS LIFESCIENCES (TAIWAN) CORPORATION.

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
f264893b9be6bc4354e66a892964cbc0
Registration Details
Taiwan FDA Registration: f264893b9be6bc4354e66a892964cbc0
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Edwards” Carpentier-Edwards PERIMOUNT Pericardial Bioprosthesis
TW: “愛德華” 卡本特-愛德華沛旅旺心包生物瓣膜
Risk Class 3
MD

Registration Details

f264893b9be6bc4354e66a892964cbc0

Ministry of Health Medical Device Import No. 025232

DHA05602523201

Company Information

United States

Product Details

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

E Cardiovascular devices

E3925 Heart valve replacement

Imported from abroad

Dates and Status

Aug 26, 2013

Aug 26, 2028