Taiwan FDA registration 290df6fb55501d3e2225b3c5ff7a7ea3

"Kabi" Lumi infusion combination set

TW: “卡比”路美輸液組合套
Taiwan flagTaiwan·Risk Class 2·CLINICO MEDICAL SP. Z.O.O. BŁONIE NEAR WROCŁAW·Registered Jul 25, 2012 – Jul 25, 2022Cancelled
Registration details
Analysis ID
290df6fb55501d3e2225b3c5ff7a7ea3
Customs Code
DHA00602390609
Company information
Manufacturer Country
Poland
Authorized Representative
FRESENIUS KABI TAIWAN LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J.5440 血管內輸液套
Import Information
import
Dates and status
Registration Date
Jul 25, 2012
Expiry Date
Jul 25, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

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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