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Richard Wolf GmbH · Model 8654996 · UDI-DI 04055207057308

FDC
10
510(k) clearances
440
Adverse events (2 deaths)
0
Recalls
37
Facilities

Description

GUIDE SHEATH LASER THERAPY 600µM 22FR with lateral guide, distal end with ring, 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.