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AndoCor Aortic Root Cannulae - Taiwan Registration 25424d559f5540c19da9d3570cfe6265

Access comprehensive regulatory information for AndoCor Aortic Root Cannulae in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 25424d559f5540c19da9d3570cfe6265 and manufactured by ANDOCOR NV. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..

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25424d559f5540c19da9d3570cfe6265
Registration Details
Taiwan FDA Registration: 25424d559f5540c19da9d3570cfe6265
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Device Details

AndoCor Aortic Root Cannulae
TW: ๆฉๅคšๅฏ‡ไธปๅ‹•่„ˆๆ น้ƒจๅฐŽ็ฎก
Risk Class 2
MD

Registration Details

25424d559f5540c19da9d3570cfe6265

Ministry of Health Medical Device Import No. 030819

DHA05603081901

Company Information

Belgium

Product Details

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

E Cardiovascular devices

E4210 Vascular catheters, cannula and tubes for cardiopulmonary vascular bypass

Imported from abroad

Dates and Status

Apr 25, 2018

Apr 25, 2023