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"Kabi" Lumi infusion combination set - Taiwan Registration 290df6fb55501d3e2225b3c5ff7a7ea3

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 290df6fb55501d3e2225b3c5ff7a7ea3 and manufactured by 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, 1 companies making similar products including 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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290df6fb55501d3e2225b3c5ff7a7ea3
Registration Details
Taiwan FDA Registration: 290df6fb55501d3e2225b3c5ff7a7ea3
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Device Details

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

Registration Details

290df6fb55501d3e2225b3c5ff7a7ea3

DHA00602390609

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

Jul 25, 2012

Jul 25, 2022

Apr 12, 2024

Cancellation Information

Logged out

許可證已逾有效期

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