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Midmark

MIDMARK CORPORATION · Model 029-5153-02 · UDI-DI 00841709108013

NRD
2
510(k) clearances
3
Adverse events
0
Recalls
146
Facilities

Description

Base unit assembly, 2000 RPM and 7 users, used on the G7 PowerVac G Dry Vacuums.

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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.