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Ventlab

VENTLAB, LLC · Model HS1050-E · UDI-DI 10889483083604

NHK Prescription
10
510(k) clearances
113
Adverse events (6 deaths)
0
Recalls
9
Facilities

Description

1/2 LITER HYPER W/MANOMETER

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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.