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GE Healthcare Finland Oy · Model D-fend Pro Water Trap, M1182629 · UDI-DI 00840682102919

CBQ BZL BZK CBR CAP CCL CBS NHQ NHP NHO CCK Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

D-FEND PRO WATER TRAP, M1182629

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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.