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HELIOS® AUTOMATED IFA SYSTEM

Aesku.Diagnostics GmbH & Co. KG · Model REF.IOS-1000 · UDI-DI 04250289512541

PIV
1
510(k) clearances
0
Adverse events
0
Recalls
10
Facilities

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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.