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Hematype Segment Device

Fresenius Kabi AG · Model 4R5128 · UDI-DI 10810020440536

KSS Prescription
6
510(k) clearances
72
Adverse events
0
Recalls
39
Facilities

Description

Hematype Segment Device

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.