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Sechrist Industries, Inc.

SECHRIST INDUSTRIES, INC. · Model 20409-10 · UDI-DI 00852682007002

ONZ
6
510(k) clearances
3
Adverse events (1 deaths)
0
Recalls
1
Facilities

Description

VENT,MILLENNIUM,ENGLISH,W/O S&P

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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.