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"Mekewei" microporous membrane oxygenator with venous hard shell blood storage tank - Taiwan Registration e653c1a1b11e3161dea800978659101c

Access comprehensive regulatory information for "Mekewei" 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 e653c1a1b11e3161dea800978659101c and manufactured by MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti;; Maquet Cardiopulmonary GmbH. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Maquet Cardiopulmonary AG; MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti, MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti;; Maquet Cardiopulmonary GmbH, and 3 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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e653c1a1b11e3161dea800978659101c
Registration Details
Taiwan FDA Registration: e653c1a1b11e3161dea800978659101c
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Device Details

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

Registration Details

e653c1a1b11e3161dea800978659101c

DHA00602183400

Product Details

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

E Cardiovascular Medicine Science

E.4400 ๅฟƒ่‚บ่ก€็ฎก็นž้“่ก“่ก€ๆถฒๅ„ฒๅญ˜ๅ™จ;; E.4350 ๅฟƒ่‚บ่ก€็ฎก็นž้“่ก“ๅ’Œๆฐงๅ™จ

import

Dates and Status

Dec 10, 2010

Dec 10, 2025

Jun 27, 2023

Cancellation Information

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