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MEIJER

MEIJER, INC. · Model 4043225 · UDI-DI 00708820010000

HHD
10
510(k) clearances
138
Adverse events
0
Recalls
314
Facilities

Description

REGULAR MAXIPAD WINGLESS UNSCENTED 48 CT

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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.