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"Meikewei" infant microporous membrane oxygenator with venous hard shell blood storage tank - Taiwan Registration e4051a021e7e1ef216078eb4bf5950ae

Access comprehensive regulatory information for "Meikewei" infant microporous membrane oxygenator with venous hard shell blood storage tank in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e4051a021e7e1ef216078eb4bf5950ae and manufactured by MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti;; MAQUET CARDIOPULMONARY AG. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti;; MAQUET CARDIOPULMONARY AG, and 1 recent registrations in the same category. 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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e4051a021e7e1ef216078eb4bf5950ae
Registration Details
Taiwan FDA Registration: e4051a021e7e1ef216078eb4bf5950ae
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Device Details

"Meikewei" infant microporous membrane oxygenator with venous hard shell blood storage tank
TW: โ€œ้‚ๆŸฏๅ”ฏโ€ๅนผๅ…’ๅพฎๅญ”่†œๆฐงๅˆๅ™จ้™„้œ่„ˆ็กฌๆฎผๅผๅ„ฒ่ก€ๆงฝ
Risk Class 2

Registration Details

e4051a021e7e1ef216078eb4bf5950ae

DHA00602282606

Product Details

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

E Cardiovascular Medicine Science

E.4350 Cardiopulmonary vascular bypass and oxygen apparatus

import

Dates and Status

Sep 29, 2011

Sep 29, 2026

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