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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle
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Device c. difficile nucleic acid amplification test assay
Regulation Description Microorganism differentiation and identification device.
Definition In vitro diagnostic test for the qualitative detection of toxigenic clostridium difficile nucleic acids isolated and purified from stool specimens obtained from symptomatic patients.
Product CodeOMN
Regulation Number 866.2660
Device Class 1

Recalls
Manufacturer Recall Class Date Posted
1 Meridian Bioscience Inc II Nov-19-2025
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