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"Meikowei" is an artificial blood vessel at the root of the aorta - Taiwan Registration 57bf4d5748a7abbc37fac3673ab1935c

Access comprehensive regulatory information for "Meikowei" is an artificial blood vessel at the root of the aorta in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 57bf4d5748a7abbc37fac3673ab1935c and manufactured by INTERVASCULAR SAS. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..

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57bf4d5748a7abbc37fac3673ab1935c
Registration Details
Taiwan FDA Registration: 57bf4d5748a7abbc37fac3673ab1935c
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Device Details

"Meikowei" is an artificial blood vessel at the root of the aorta
TW: โ€œ้‚ๆŸฏๅ”ฏโ€่‹ฑ็‰นไฝณไธปๅ‹•่„ˆๆ น้ƒจไบบๅทฅ่ก€็ฎก
Risk Class 2

Registration Details

57bf4d5748a7abbc37fac3673ab1935c

DHA00602390507

Company Information

France

Product Details

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

E Cardiovascular Medicine Science

E.3450 ่ก€็ฎก็งปๆคๅฝŒ่ฃœ็‰ฉ

import

Dates and Status

Jul 24, 2012

Jul 24, 2027