Intended Use
This kit is an enzyme immunoassay (EIA) system intended for in
vitro diagnostic use for qualitative detection of
Legionella pneumophila serogroup 1 antigen in human urine
as an adjunct to culture for the presumptive diagnosis of past or
current Legionnaires’ disease.
This product is FDA-Cleared and CE Marked.
Product Details
- Availability – Global
- CLIA Status – Moderately Complex
- Sample type – Urine
- Time for test results – Three (3) hours
- Sensitivity – 97.7%
- Specificity – 100%
Catalog Number
- 851-000 (96 well test kit)
Product Information
Ordering Information