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"Meikewei" cardiopulmonary cardiopulmonary bypass tubing group - Taiwan Registration f55edf0dc548bc0c5b085d48c9dfc5b1

Access comprehensive regulatory information for "Meikewei" cardiopulmonary cardiopulmonary bypass tubing group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f55edf0dc548bc0c5b085d48c9dfc5b1 and manufactured by MAQUET CARDIOPLUMONARY MEDIKAL TEKNIK SAN. TIC LTD. STI;; Maquet Cardiopulmonary GmbH. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..

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f55edf0dc548bc0c5b085d48c9dfc5b1
Registration Details
Taiwan FDA Registration: f55edf0dc548bc0c5b085d48c9dfc5b1
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Device Details

"Meikewei" cardiopulmonary cardiopulmonary bypass tubing group
TW: โ€œ้‚ๆŸฏๅ”ฏโ€ๅฟƒ่‚บ้ซ”ๅค–ๅพช็’ฐ็ฎก่ทฏ็ต„
Risk Class 2
Cancelled

Registration Details

f55edf0dc548bc0c5b085d48c9dfc5b1

DHA00602022904

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing

import

Dates and Status

Oct 07, 2009

Oct 07, 2019

Jun 16, 2022

Cancellation Information

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