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“LivaNova” FlexFlow Venous Cannula - Taiwan Registration 64660cbee8b5be8783013e4187c96066

Access comprehensive regulatory information for “LivaNova” FlexFlow Venous Cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 64660cbee8b5be8783013e4187c96066 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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64660cbee8b5be8783013e4187c96066
Registration Details
Taiwan FDA Registration: 64660cbee8b5be8783013e4187c96066
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Device Details

“LivaNova” FlexFlow Venous Cannula
TW: “里凡諾瓦”菲樂流靜脈導管
Risk Class 2
MD

Registration Details

64660cbee8b5be8783013e4187c96066

Ministry of Health Medical Device Import No. 027310

DHA05602731002

Company Information

United States

Product Details

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

E Cardiovascular devices

E4210 Vascular catheters, cannula and tubes for cardiopulmonary vascular bypass

Imported from abroad

Dates and Status

May 28, 2015

May 28, 2025