"Kabi" Aimeco blood component separator
Taiwan·Risk Class 2·Fresenius Kabi AG;; PLEXUS MANUFACTURING SDN. BHD.·Registered Apr 05, 2018 – Apr 05, 2023Expired- Analysis ID
- 1eac338d8a0bf627cc4aab2343eec17e
- Customs Code
- DHA05603053701
- Manufacturer Country
- Malaysia;;Germany
- Authorized Representative
- FRESENIUS KABI TAIWAN LIMITED
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9245 Automated hemocytoseparator
- Import Information
- Input;; Contract manufacturing
- Registration Date
- Apr 05, 2018
- Expiry Date
- Apr 05, 2023
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Access comprehensive regulatory information for "Kabi" Aimeco blood component separator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1eac338d8a0bf627cc4aab2343eec17e and manufactured by Fresenius Kabi AG;; PLEXUS MANUFACTURING SDN. BHD.. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FRESENIUS KABI AG;; Fresenius HemoCare GmbH, and 1 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.