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“Terumo” Capiox RX Oxygenator - Taiwan Registration c76984854a9b499752f65cc53f102d5d

Access comprehensive regulatory information for “Terumo” Capiox RX Oxygenator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c76984854a9b499752f65cc53f102d5d and manufactured by TERUMO CARDIOVASCULAR SYSTEMS CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL 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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c76984854a9b499752f65cc53f102d5d
Registration Details
Taiwan FDA Registration: c76984854a9b499752f65cc53f102d5d
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Device Details

“Terumo” Capiox RX Oxygenator
TW: “泰爾茂” 氧合器
Risk Class 2
MD

Registration Details

c76984854a9b499752f65cc53f102d5d

Ministry of Health Medical Device Import No. 034318

DHA05603431809

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular devices

E4350 Cardiopulmonary vascular bypass and oxygen apparatus

Imported from abroad

Dates and Status

Feb 01, 2021

Feb 01, 2026