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"McKewei" artificial heart-lung machine - Taiwan Registration 8ed520dcd80a6f723c0239e1b7cf23e0

Access comprehensive regulatory information for "McKewei" artificial heart-lung machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8ed520dcd80a6f723c0239e1b7cf23e0 and manufactured by MEDIKOMP 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 CRITICAL CARE AB, 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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8ed520dcd80a6f723c0239e1b7cf23e0
Registration Details
Taiwan FDA Registration: 8ed520dcd80a6f723c0239e1b7cf23e0
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Device Details

"McKewei" artificial heart-lung machine
TW: โ€œ้‚ๆŸฏๅ”ฏโ€ไบบๅทฅๅฟƒ่‚บๆฉŸ
Risk Class 2

Registration Details

8ed520dcd80a6f723c0239e1b7cf23e0

DHA00601928705

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.4220 ๅฟƒ่‚บ่ก€็ฎก็นž้“่ก“ไน‹ๅฟƒ่‚บๆฉŸ

Input;; Contract manufacturing

Dates and Status

Oct 22, 2008

Oct 22, 2023

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