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"Kabi" Aimeko Blood Separation Set - Taiwan Registration a99291cf666bbb17596cab853a1d4c6c

Access comprehensive regulatory information for "Kabi" Aimeko Blood Separation Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a99291cf666bbb17596cab853a1d4c6c and manufactured by Fresenius Kabi AG;; Fenwal International, Inc.. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.

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a99291cf666bbb17596cab853a1d4c6c
Registration Details
Taiwan FDA Registration: a99291cf666bbb17596cab853a1d4c6c
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Device Details

"Kabi" Aimeko Blood Separation Set
TW: โ€œๅกๆฏ”โ€ๆ„›็พŽๅฏ่ก€ๆถฒๅˆ†้›ขๅฅ—็ต„
Risk Class 2

Registration Details

a99291cf666bbb17596cab853a1d4c6c

DHA05603114107

Company Information

Dominican Republic;;Germany

Product Details

This product can only be used with the AmiCORE Blood Fractionator for the collection of reduced leukoapheresis platelets (LRAP).

B Hematology, pathology, and genetics

B.9100 Containers for the collection and disposal of blood and blood components

import

Dates and Status

Jun 07, 2018

Jun 07, 2028