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Healy

Healy GmbH · Model 0006 · UDI-DI 04251784906101

NUH

510(k) clearances

118

Adverse events

Recalls

169

Facilities

Description

The device is a variant of the Healy device with primary DI number 04251784906033. This device is available in Wave format instead of the standard whit color.

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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.