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VITEK® REVEAL™ SEALER

BIOMERIEUX , INC. · Model 900-00003 · UDI-DI 00860007326912

SAN Prescription
1
510(k) clearances
2
Adverse events
0
Recalls
7
Facilities

Description

The VITEK REVEAL SEALER provides the heat welding of the VITEK REVEAL SENSOR PANEL to the 96 well AST Drug Plate.

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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.