"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.
Device Details
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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"Meikewei" microporous membrane oxygenator
Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH
1ef5786ba6e965a4fa954607fcb0e6c8
2
"Meikewei" microporous membrane oxygenator
Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH
5586b5bf1d7a179b90b673750d45bdf2
2
"Meikewei" microporous membrane oxygenator
Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH
0c2b0709f39563ae44e4db7d5ec9329a
2

