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Richard Wolf GmbH · Model 8934175 · UDI-DI 04055207022740

FEC

510(k) clearances

Adverse events (1 deaths)

Recalls

Facilities

Description

OBTURATOR DULL Ø 10MM TL 224MM TL 224mm, for 8923.016 and 8934.901, reusable

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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.