"Kabi" Lumi infusion combination set
- Analysis ID
- daaf0a74cf0d60f9fa1728649c840c8f
- Customs Code
- DHA05603431006
- Manufacturer Country
- Germany;;Poland
- Authorized Representative
- FRESENIUS KABI TAIWAN LIMITED
- 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
- Registration Date
- Jan 25, 2021
- Expiry Date
- Jan 25, 2026
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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.