Taiwan FDA registration 579c9bafc2d7c2412b9fa003bfc8ac3b
"Kabi" Wei all-round infusion system software
TW: “卡比”威全能輸液系統軟體
Taiwan·Risk Class 2·Fresenius Vial S.A.S.;; Fresenius Kabi AG·Registered Sep 10, 2020 – Sep 10, 2025ExpiredRegistration details
- Analysis ID
- 579c9bafc2d7c2412b9fa003bfc8ac3b
- Customs Code
- DHA05603394801
Company information
- Manufacturer
- Fresenius Vial S.A.S.;; Fresenius Kabi AG
- Manufacturer Country
- France;;Germany
- 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.5725 Infusion 幫浦
- Import Information
- import
Dates and status
- Registration Date
- Sep 10, 2020
- Expiry Date
- Sep 10, 2025
About this record
Access comprehensive regulatory information for "Kabi" Wei all-round infusion system software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 579c9bafc2d7c2412b9fa003bfc8ac3b and manufactured by Fresenius Vial S.A.S.;; Fresenius Kabi AG. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.
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