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ADITEK

ADITEK DO BRASIL S/A · Model 05.04.0836 · UDI-DI 07899439293199

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510(k) clearances
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Facilities

Description

100 Kits 7x7 BioMax 022 MBT 3,4,5 w/2800

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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.