Taiwan FDA registration 746ed7bd01a0197da862b4936c3c5cf6
"Kabi" Lumi infusion sleeve
TW: “卡比”路美輸液套
Registration details
- Analysis ID
- 746ed7bd01a0197da862b4936c3c5cf6
- Customs Code
- DHA05602868804
Company information
- Manufacturer Country
- Germany;;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 13, 2016
- Expiry Date
- Jul 13, 2026
About this record
Access comprehensive regulatory information for "Kabi" Lumi infusion sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 746ed7bd01a0197da862b4936c3c5cf6 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.
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