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ADVIA Centaur AMH Kit

Siemens Healthcare Diagnostics Inc. · Model 10998432 · UDI-DI 00630414225692

PQO
1
510(k) clearances
14
Adverse events
1
Recalls
9
Facilities

Description

AMH - Centaur - RGT – 100T

Recalls

DateFirmReason
2025-11-03GET TESTED INTERNATIONAL ABDistribution without premarket approval/clearance.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.