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“Edwards” IntraClude Intra-Aortic Occlusion Device - Taiwan Registration 1a48058967544900fe516601ea4e0d7b

Access comprehensive regulatory information for “Edwards” IntraClude Intra-Aortic Occlusion Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1a48058967544900fe516601ea4e0d7b 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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1a48058967544900fe516601ea4e0d7b
Registration Details
Taiwan FDA Registration: 1a48058967544900fe516601ea4e0d7b
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Device Details

“Edwards” IntraClude Intra-Aortic Occlusion Device
TW: “愛德華”主動脈阻塞導管
Risk Class 2
MD
Cancelled

Registration Details

1a48058967544900fe516601ea4e0d7b

Ministry of Health Medical Device Import No. 026414

DHA05602641409

Company Information

United States

Product Details

E Cardiovascular devices

E4450 Vascular Clip

Imported from abroad

Dates and Status

Jul 29, 2014

Jul 29, 2019

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者