Taiwan FDA registration 25699e378e206ba9fdbca73c5bc2246e

"Kabi" Combo Blood Bag Group with Filter

TW: “卡比” 康博含濾器血袋組

Taiwan·Risk Class 2·Fresenius Kabi AG;; Fresenius Kabi Horatev CZ s.r.o.·Registered Oct 14, 2021 – Oct 14, 2026Active

Registration details

Analysis ID: 25699e378e206ba9fdbca73c5bc2246e
Customs Code: DHA05603491402

Company information

Manufacturer: Fresenius Kabi AG;; Fresenius Kabi Horatev CZ s.r.o.
Manufacturer Country: Germany;;Czechia
Authorized Representative: FRESENIUS KABI TAIWAN LIMITED

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.9100 Containers for the collection and disposal of blood and blood components
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Oct 14, 2021
Expiry Date: Oct 14, 2026

About this record

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.

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