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RAZEK EQUIPAMENTOS

RAZEK EQUIPAMENTOS LTDA · Model 738941720 · UDI-DI 07908882817057

LXH
10
510(k) clearances
82,132
Adverse events (55 deaths)
0
Recalls
1,119
Facilities

Description

Razek Surgical Burrs - BP155W (1,9)

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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.