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"Fresenius" acute treatment system connector - Taiwan Registration 273f720eb7a670e48269c5951df80cf9

Access comprehensive regulatory information for "Fresenius" acute treatment system connector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 273f720eb7a670e48269c5951df80cf9 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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273f720eb7a670e48269c5951df80cf9
Registration Details
Taiwan FDA Registration: 273f720eb7a670e48269c5951df80cf9
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Device Details

"Fresenius" acute treatment system connector
TW: โ€œ่ฒปๆฃฎๅฐคๆ–ฏโ€ๆ€ฅๆ€งๆฒป็™‚็ณป็ตฑ้€ฃๆŽฅ้ ญ
Risk Class 2

Registration Details

273f720eb7a670e48269c5951df80cf9

DHA00601805709

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

May 07, 2007

May 07, 2027