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"Fresenius" multiplex filtration high-volume venous hemofiltration rehydration circuit group - Taiwan Registration 28eba776beb7142d12a0d0eebf6f07d2

Access comprehensive regulatory information for "Fresenius" multiplex filtration high-volume venous hemofiltration rehydration circuit group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 28eba776beb7142d12a0d0eebf6f07d2 and manufactured by Nova Med GmbH Antalya Free Zone Central Branch; Fresenius Medical Care AG & Co. KGaA. The authorized representative in Taiwan is FRESENIUS MEDICAL CARE TAIWAN CO., LTD..

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28eba776beb7142d12a0d0eebf6f07d2
Registration Details
Taiwan FDA Registration: 28eba776beb7142d12a0d0eebf6f07d2
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Device Details

"Fresenius" multiplex filtration high-volume venous hemofiltration rehydration circuit group
TW: โ€œ่ฒปๆฃฎๅฐคๆ–ฏโ€ๅคš้‡้Žๆฟพ้ซ˜ๅฎน็ฉ้œ่„ˆ่ก€ๆถฒ้Žๆฟพ่ฃœๆถฒ่ฟด่ทฏ็ต„
Risk Class 2

Registration Details

28eba776beb7142d12a0d0eebf6f07d2

DHA00601797809

Company Information

Product Details

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

H Gastroenterology and urology

H.5540 Blood Access Devices and Accessories

import

Dates and Status

Apr 03, 2007

Apr 03, 2027