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"Kabi" Combo Blood Bag Group with Filter - Taiwan Registration 25699e378e206ba9fdbca73c5bc2246e

Access comprehensive regulatory information for "Kabi" Combo Blood Bag Group with Filter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 25699e378e206ba9fdbca73c5bc2246e and manufactured by Fresenius Kabi AG;; Fresenius Kabi Horatev CZ s.r.o.. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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25699e378e206ba9fdbca73c5bc2246e
Registration Details
Taiwan FDA Registration: 25699e378e206ba9fdbca73c5bc2246e
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Device Details

"Kabi" Combo Blood Bag Group with Filter
TW: โ€œๅกๆฏ”โ€ ๅบทๅšๅซๆฟพๅ™จ่ก€่ข‹็ต„
Risk Class 2

Registration Details

25699e378e206ba9fdbca73c5bc2246e

DHA05603491402

Company Information

Product Details

Details are as detailed as approved Chinese instructions

B Hematology, pathology, and genetics

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

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Oct 14, 2021

Oct 14, 2026