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“Terumo” Capiox FX advance Oxygenator - Taiwan Registration dd857d4bffe9cc13a74dab9b6ebd4f3e

Access comprehensive regulatory information for “Terumo” Capiox FX advance Oxygenator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dd857d4bffe9cc13a74dab9b6ebd4f3e and manufactured by TERUMO CARDIOVASCULAR SYSTEMS CORP.. 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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Registration Details
Taiwan FDA Registration: dd857d4bffe9cc13a74dab9b6ebd4f3e
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Device Details

“Terumo” Capiox FX advance Oxygenator
TW: “泰爾茂” 菲斯新一代氧合器
Risk Class 2
MD

Registration Details

dd857d4bffe9cc13a74dab9b6ebd4f3e

Ministry of Health Medical Device Import No. 034488

DHA05603448808

Company Information

United States

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

Apr 07, 2021

Apr 07, 2026