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VACU-TEC CUVETTE-L

DIESSE DIAGNOSTICA SENESE SPA · Model 10208 · UDI-DI 08033891320645

GHC
1
510(k) clearances
32
Adverse events
1
Recalls
17
Facilities

Recalls

DateFirmReason
2010-04-12Vital Diagnostics, Inc.The tube may fall out or separate from the Slider adapter

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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.