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"Rivanova" vascular cannula - Taiwan Registration ec241e702e15e2c2a9c37210bf8353bd

Access comprehensive regulatory information for "Rivanova" vascular cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ec241e702e15e2c2a9c37210bf8353bd and manufactured by LivaNova USA, Inc.. The authorized representative in Taiwan is INTERLINK MEDICAL ENTERPRISE 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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ec241e702e15e2c2a9c37210bf8353bd
Registration Details
Taiwan FDA Registration: ec241e702e15e2c2a9c37210bf8353bd
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Device Details

"Rivanova" vascular cannula
TW: โ€œ้‡Œๅ‡ก่ซพ็“ฆโ€่ก€็ฎกๅฅ—็ฎก
Risk Class 2

Registration Details

ec241e702e15e2c2a9c37210bf8353bd

DHA00601923308

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing

import

Dates and Status

Sep 25, 2008

Sep 25, 2028