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"Kabi" Lumi infusion combination set - Taiwan Registration ff730176443962a178dbc91531af5266

Access comprehensive regulatory information for "Kabi" Lumi infusion combination set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ff730176443962a178dbc91531af5266 and manufactured by Fresenius Kabi AG;; CLINICO MEDICAL SP. Z.O.O. BŁONIE NEAR WROCŁAW. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Fresenius Kabi AG;; CLINICO MEDICAL SP. Z.O.O. BŁONIE NEAR WROCŁAW, CLINICO MEDICAL SP. Z.O.O. BŁONIE NEAR WROCŁAW, and 2 recent registrations in the same category. 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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ff730176443962a178dbc91531af5266
Registration Details
Taiwan FDA Registration: ff730176443962a178dbc91531af5266
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Device Details

"Kabi" Lumi infusion combination set
TW: “卡比”路美輸液組合套
Risk Class 2

Registration Details

ff730176443962a178dbc91531af5266

DHA05603289600

Company Information

Product Details

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

J General hospital and personal use equipment

J.5440 血管內輸液套

import

Dates and Status

Oct 17, 2019

Oct 17, 2029