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"EUROSETS" Cardiopulmonary bypass accessory equipment (Non-Sterile) - Taiwan Registration 97bbaad0b80ad5eb43aab39b018451d5

Access comprehensive regulatory information for "EUROSETS" Cardiopulmonary bypass accessory equipment (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 97bbaad0b80ad5eb43aab39b018451d5 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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97bbaad0b80ad5eb43aab39b018451d5
Registration Details
Taiwan FDA Registration: 97bbaad0b80ad5eb43aab39b018451d5
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Device Details

"EUROSETS" Cardiopulmonary bypass accessory equipment (Non-Sterile)
TW: "ๅ„ชๆจ‚" ๅฟƒ่‚บ่ก€็ฎก็นž้“่ก“่ผ”ๅŠฉ่จญๅ‚™ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

97bbaad0b80ad5eb43aab39b018451d5

Ministry of Health Medical Device Import No. 022293

DHA09402229300

Company Information

Italy

Product Details

Limited to the first level recognition range of medical equipment management measures cardiopulmonary vascular bypass auxiliary equipment (E.4200).

E Cardiovascular devices

E4200 Cardiopulmonary vascular bypass assistive device

Imported from abroad

Dates and Status

Feb 03, 2021

Feb 03, 2026