"Kabi" Aimeco blood component separator - Taiwan Registration 1eac338d8a0bf627cc4aab2343eec17e
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.
Device Details
Registration Details
1eac338d8a0bf627cc4aab2343eec17e
DHA05603053701
Product Details
For details, it is Chinese approved copy of the imitation order.
B Hematology, pathology, and genetics
B.9245 Automated hemocytoseparator
Input;; Contract manufacturing
Dates and Status
Apr 05, 2018
Apr 05, 2023