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Dna-Reagents, Cytomegalovirus

FDA product code LSO · Class 2 · Microbiology

0
Registered devices
2
Adverse events
1
Recalls
0
510(k) clearances

Recent recalls

DateFirmReason
2004-05-28Digene CorpIn vitro diagnostic test kit may produce false negative clinical results.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.