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"Kabi" Lumi infusion combination set - Taiwan Registration daaf0a74cf0d60f9fa1728649c840c8f

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 daaf0a74cf0d60f9fa1728649c840c8f 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 CLINICO MEDICAL SP. Z.O.O. BŁONIE NEAR WROCŁAW, Fresenius Kabi AG;; 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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daaf0a74cf0d60f9fa1728649c840c8f
Registration Details
Taiwan FDA Registration: daaf0a74cf0d60f9fa1728649c840c8f
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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

daaf0a74cf0d60f9fa1728649c840c8f

DHA05603431006

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

Jan 25, 2021

Jan 25, 2026