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Kendall
Cardinal Health 200, LLC · Model 41556 · UDI-DI 20192253052883
10
510(k) clearances
67
Adverse events
0
Recalls
126
Facilities
Description
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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.
