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PNEUMOCLEAR

W.O.M. World of Medicine GmbH · Model FM300 · UDI-DI 04056702003456

OSV HIF

510(k) clearances

Adverse events

Recalls

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.