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"McKovei" double vena vein drainage perfusion catheter - Taiwan Registration 3cb6e2f2cb38b1794ce788ea71cc7e0d

Access comprehensive regulatory information for "McKovei" double vena vein drainage perfusion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3cb6e2f2cb38b1794ce788ea71cc7e0d and manufactured by MAQUET CARDIOPLUMONARY MEDIKAL TEKNIK SAN. TIC LTD. STI;; MAQUET CARDIOPULMONARY AG. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..

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3cb6e2f2cb38b1794ce788ea71cc7e0d
Registration Details
Taiwan FDA Registration: 3cb6e2f2cb38b1794ce788ea71cc7e0d
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Device Details

"McKovei" double vena vein drainage perfusion catheter
TW: โ€œ้‚ๆŸฏๅ”ฏโ€้›™่…”้œ่„ˆๅผ•ๆต็ŒๆณจๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

3cb6e2f2cb38b1794ce788ea71cc7e0d

DHA00602053409

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

Jan 18, 2010

Jan 18, 2020

Jun 16, 2022

Cancellation Information

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