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"Rivanova" ductus arteriosus - Taiwan Registration e8f3132a452cfd320e590e5196da8402

Access comprehensive regulatory information for "Rivanova" ductus arteriosus in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e8f3132a452cfd320e590e5196da8402 and manufactured by LivaNova USA, Inc.. The authorized representative in Taiwan is INTERLINK MEDICAL ENTERPRISE CO., LTD..

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e8f3132a452cfd320e590e5196da8402
Registration Details
Taiwan FDA Registration: e8f3132a452cfd320e590e5196da8402
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Device Details

"Rivanova" ductus arteriosus
TW: โ€œ้‡Œๅ‡ก่ซพ็“ฆโ€ๅ‹•่„ˆๅฐŽ็ฎก
Risk Class 2

Registration Details

e8f3132a452cfd320e590e5196da8402

DHA00602064801

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

Mar 10, 2010

Mar 10, 2030