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DigiDop

NEWMAN MEDICAL LLC · Model DD-300-D2 · UDI-DI 00852785008005

LXE Prescription
1
510(k) clearances
8
Adverse events (1 deaths)
0
Recalls
1
Facilities

Description

DigiDop 300, non-display, 2MHZ OB

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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.