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“Edwards” OptiSite Arterial Perfusion Cannula - Taiwan Registration 37ab0c56034bb15a2bdf1789fea1fec7

Access comprehensive regulatory information for “Edwards” OptiSite Arterial Perfusion Cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 37ab0c56034bb15a2bdf1789fea1fec7 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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37ab0c56034bb15a2bdf1789fea1fec7
Registration Details
Taiwan FDA Registration: 37ab0c56034bb15a2bdf1789fea1fec7
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Device Details

“Edwards” OptiSite Arterial Perfusion Cannula
TW: “愛德華”動脈灌注導管
Risk Class 2
MD

Registration Details

37ab0c56034bb15a2bdf1789fea1fec7

Ministry of Health Medical Device Import No. 025230

DHA05602523007

Company Information

United States

Product Details

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

E Cardiovascular devices

E1300 catheter cannula

Imported from abroad

Dates and Status

Aug 15, 2013

Aug 15, 2028