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TUBE, CAPILLARY, VETERINARY, (BUNDLE 50)

Epocal Inc · Model AT-0007-00-00 · UDI-DI 00809708049232

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510(k) clearances
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Adverse events
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Facilities

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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.