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n.a.

Karl Storz GmbH & Co. KG · Model 50207BG · UDI-DI 04048551170380

GCM Prescription

510(k) clearances

1,571

Adverse events (1 deaths)

Recalls

Facilities

Description

Suction and Irrigation Tube, curved

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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.