"Kabi" Wei all-round infusion system software - Taiwan Registration 579c9bafc2d7c2412b9fa003bfc8ac3b
Access comprehensive regulatory information for "Kabi" Wei all-round infusion system software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 579c9bafc2d7c2412b9fa003bfc8ac3b and manufactured by Fresenius Vial S.A.S.;; Fresenius Kabi AG. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details. 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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579c9bafc2d7c2412b9fa003bfc8ac3b
Registration Details
Taiwan FDA Registration: 579c9bafc2d7c2412b9fa003bfc8ac3b
Device Details
"Kabi" Wei all-round infusion system software
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Risk Class 2

