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"Kabi" Aimeco blood component separator - Taiwan Registration e5da2cdf803d1ce7678f2f1beeef375c

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 e5da2cdf803d1ce7678f2f1beeef375c and manufactured by FRESENIUS KABI AG;; Fresenius HemoCare GmbH. 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;; PLEXUS MANUFACTURING SDN. BHD., 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.

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e5da2cdf803d1ce7678f2f1beeef375c
Registration Details
Taiwan FDA Registration: e5da2cdf803d1ce7678f2f1beeef375c
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Device Details

"Kabi" Aimeco blood component separator
TW: โ€œๅกๆฏ”โ€ ๆ„›็พŽๅฏ่ก€ๆถฒๆˆไปฝๅˆ†้›ขๆฉŸ
Risk Class 2

Registration Details

e5da2cdf803d1ce7678f2f1beeef375c

DHA05603620506

Company Information

Product Details

This product is an automated cytoplasmic separator suitable for collecting blood components, this product can only be used in conjunction with the AmiCORE Apheresis Kit to collect and subtract white blood cell platelets.

B Hematology, pathology, and genetics

B.9245 Automated hemocytoseparator

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jul 27, 2023

Jul 27, 2028

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