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Pumpmatic
Ashton Pumpmatic, Inc. · Model 205 · UDI-DI 00689519002059
0
510(k) clearances
0
Adverse events
0
Recalls
8
Facilities
Description
205
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Get your free API keyRead the docsData 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.
