Taiwan FDA registration 47f0bf139091514297be65e098ff51a5
"Bifu" plasma separation sleeve
TW: "比孚"血漿分離套
Taiwan·Risk Class 2·Fresenius Kabi AG;; Fenwal International, Inc.·Registered Dec 19, 2006 – Dec 19, 2026ActiveRegistration details
- Analysis ID
- 47f0bf139091514297be65e098ff51a5
- Customs Code
- DHA00601752205
Company information
- Manufacturer
- Fresenius Kabi AG;; Fenwal International, Inc.
- Manufacturer Country
- Dominican Republic;;Germany
- Authorized Representative
- Fresenius Kabi, Taiwan Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5830 Instruments for automatic blood transfer
- Import Information
- import
Dates and status
- Registration Date
- Dec 19, 2006
- Expiry Date
- Dec 19, 2026
About this record
Access comprehensive regulatory information for "Bifu" plasma separation sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 47f0bf139091514297be65e098ff51a5 and manufactured by Fresenius Kabi AG;; Fenwal International, Inc.. The authorized representative in Taiwan is Fresenius Kabi, Taiwan Co., Ltd.
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