NeuroMAUDE
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Merit Medical Avanti +

No active recall

Manufacturer: Merit Medical  · FDA product code: DRE  · Category: Dilator, Vessel, For Percutaneous Catheterization

Severity Snapshot

17 total reports2012-022022-11 date range29.4% physician / facility reported70.6% manufacturer reported3 SKU variants

Reporting Trend

Annual Reporting Volume

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Note: the 2018 Voluntary Malfunction Summary Reporting expansion means volume increases may reflect surveillance changes, not increased device risk.

Reported Events

Submitted to FDA MAUDE by physicians, hospitals, manufacturers, and patients.

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