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"Rivanova" Reb femoral venous catheter - Taiwan Registration e4ab8b2125c26fc99ca76b3ddd45e2a6

Access comprehensive regulatory information for "Rivanova" Reb femoral venous catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e4ab8b2125c26fc99ca76b3ddd45e2a6 and manufactured by LivaNova USA, Inc.. The authorized representative in Taiwan is INTERLINK MEDICAL ENTERPRISE CO., LTD..

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e4ab8b2125c26fc99ca76b3ddd45e2a6
Registration Details
Taiwan FDA Registration: e4ab8b2125c26fc99ca76b3ddd45e2a6
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Device Details

"Rivanova" Reb femoral venous catheter
TW: โ€œ้‡Œๅ‡ก่ซพ็“ฆโ€้›ทๅœ่‚ก้œ่„ˆๅฐŽ็ฎก
Risk Class 2

Registration Details

e4ab8b2125c26fc99ca76b3ddd45e2a6

DHA00602206905

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

Feb 23, 2011

Feb 23, 2026