Pure Global

"Rivanova" cardiopulmonary vascular bypass aid device (unsterilized) - Taiwan Registration cd96dbfcd87f3ee3d9e2b67d4b514c58

Access comprehensive regulatory information for "Rivanova" cardiopulmonary vascular bypass aid device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cd96dbfcd87f3ee3d9e2b67d4b514c58 and manufactured by LivaNova Deutschland GmbH. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
cd96dbfcd87f3ee3d9e2b67d4b514c58
Registration Details
Taiwan FDA Registration: cd96dbfcd87f3ee3d9e2b67d4b514c58
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Rivanova" cardiopulmonary vascular bypass aid device (unsterilized)
TW: "้‡Œๅ‡ก่ซพ็“ฆ"ๅฟƒ่‚บ่ก€็ฎก็นž้“่ก“่ผ”ๅŠฉ่จญๅ‚™ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

cd96dbfcd87f3ee3d9e2b67d4b514c58

DHA04400893000

Company Information

Germany

Product Details

It is limited to the first level identification scope of cardiopulmonary vascular bypass auxiliary equipment (E.4200) of the classification and grading management measures for medical devices.

E Cardiovascular Medicine Science

E.4200 ๅฟƒ่‚บ่ก€็ฎก็นž้“่ก“่ผ”ๅŠฉ่จญๅ‚™

import

Dates and Status

Jun 21, 2010

Jun 21, 2025