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Brasseler USA

Peter Brasseler Holdings, LLC · Model 5023416U0 · UDI-DI 00887919682134

EMN Prescription

510(k) clearances

Adverse events

Recalls

223

Facilities

Description

SJ30/336 JACQ #6 HDL 1P

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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.