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“Edwards” EndoVent Pulmonary Catheter - Taiwan Registration 5f72d56e704e362955da14da274d8781

Access comprehensive regulatory information for “Edwards” EndoVent Pulmonary Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5f72d56e704e362955da14da274d8781 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.

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5f72d56e704e362955da14da274d8781
Registration Details
Taiwan FDA Registration: 5f72d56e704e362955da14da274d8781
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Device Details

“Edwards” EndoVent Pulmonary Catheter
TW: “愛德華” 恩度凡肺動脈導管
Risk Class 2
MD

Registration Details

5f72d56e704e362955da14da274d8781

Ministry of Health Medical Device Import No. 025422

DHA05602542203

Company Information

United States

Product Details

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

E Cardiovascular devices

E1240 flow guide duct

Imported from abroad

Dates and Status

Oct 01, 2013

Oct 01, 2023