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PRO-TECH

Hi-Dow International Incorporated · Model HD-5N-N · UDI-DI 00851640007405

NUH NGX

510(k) clearances

119

Adverse events

Recalls

173

Facilities

Description

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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.