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"Meikewei" microporous membrane oxygenator - Taiwan Registration 9c2268b23b75b7c829fd08e7e226610a

Access comprehensive regulatory information for "Meikewei" microporous membrane oxygenator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9c2268b23b75b7c829fd08e7e226610a and manufactured by Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH. 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 GmbH;; 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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9c2268b23b75b7c829fd08e7e226610a
Registration Details
Taiwan FDA Registration: 9c2268b23b75b7c829fd08e7e226610a
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Device Details

"Meikewei" microporous membrane oxygenator
TW: โ€œ้‚ๆŸฏๅ”ฏโ€ๅพฎๅญ”่†œๆฐงๅˆๅ™จ
Risk Class 2
Cancelled

Registration Details

9c2268b23b75b7c829fd08e7e226610a

DHA00602020006

Company Information

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 25, 2009

Sep 25, 2024

Jun 27, 2023

Cancellation Information

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