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"Eurosets"Kompass Adult Oxygenator - Taiwan Registration fe02b4dc639762e5cfee71d96b79e0d7

Access comprehensive regulatory information for "Eurosets"Kompass Adult Oxygenator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fe02b4dc639762e5cfee71d96b79e0d7 and manufactured by EUROSETS S.r.l.. The authorized representative in Taiwan is CHAMP MEDICS 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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fe02b4dc639762e5cfee71d96b79e0d7
Registration Details
Taiwan FDA Registration: fe02b4dc639762e5cfee71d96b79e0d7
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Device Details

"Eurosets"Kompass Adult Oxygenator
TW: "ๅ„ชๆจ‚"ๅŽๅธ•ๆ€ๆˆไบบๆฐงๅˆๅ™จ
Risk Class 2
MD

Registration Details

fe02b4dc639762e5cfee71d96b79e0d7

Ministry of Health Medical Device Import No. 034744

DHA05603474400

Company Information

Italy

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular devices

E4350 Cardiopulmonary vascular bypass and oxygen apparatus

Imported from abroad

Dates and Status

Jun 25, 2021

Jun 25, 2026