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Karl Storz GmbH & Co. KG · Model 041150-20 · UDI-DI 04048438005170

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510(k) clearances

Adverse events

Recalls

Facilities

Description

Cover, with elastic tip

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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.