Taiwan FDA registration 1a7d498f51be23097a78a9f6b64a83b1
"Kirby" Aiteyi automatic autologous blood salvage system kit
TW: “卡比” 艾特易全自動自體血液回收系統套組
Taiwan·Risk Class 2·Fresenius Kabi AG;; Fenwal International, Inc.·Registered Jun 02, 2024 – Jun 02, 2029ActiveRegistration details
- Analysis ID
- 1a7d498f51be23097a78a9f6b64a83b1
- Customs Code
- DHA05603721300
Company information
- Manufacturer
- Fresenius Kabi AG;; Fenwal International, Inc.
- Manufacturer Country
- Dominican Republic;;Germany
- Authorized Representative
- FRESENIUS KABI TAIWAN LIMITED
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- Jun 02, 2024
- Expiry Date
- Jun 02, 2029
About this record
Access comprehensive regulatory information for "Kirby" Aiteyi automatic autologous blood salvage system kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1a7d498f51be23097a78a9f6b64a83b1 and manufactured by Fresenius Kabi AG;; Fenwal International, Inc.. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.
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