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MODO

NIHON KOHDEN AMERICA, INC. · Model A/NIH8000 · UDI-DI 00841983103704

OLT Prescription
10
510(k) clearances
35
Adverse events (2 deaths)
0
Recalls
67
Facilities

Description

CART FOR EEG-9200 / EEG-1200

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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.