Biomed Diagnostics, Inc. products
Clinical Microbiology - Prepared Culture Media
Biomed - Nasopharyngeal (NP) or Oropharyngeal (OP) Synthetic Fiber Swab
The Saline Solution (0.85%) is an isotonic solution, manufactured in compliance with ISO 13485:2016 standards. It is intended to be inoculated with nasopharyngeal (NP) or oropharyngeal (OP) synthetic fiber swab specimens (Not provided, see IFU for details), to be analyzed in the laboratory with validated qRT-PCR assays. This Saline Solution (0.85%) has been validated for the detection of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that causes COVID-19 disease in humans.1,2 The use of this device for other viral specimens is the responsibility of the end user including the validation thereof.
Biomed InTray - Model GC - Selective Media
Neisseria gonorrhoeae is a common sexually transmitted disease organism broadly disseminated throughout the world. InTray GC is a fully enclosed microbiology cassette, which enables sample collection, transport, culture and identification in a single unit. The proprietary modified Thayer Martin agar is selective for gonococcal bacteria. Results can be interpreted after 24-72 hours incubation. InTray GC is a single exposure culture system with dynamic built-in components and features that are designed for user compatibility and ease of detection.
Food and Environmental Microbiology - Prepared Culture Media
Intray Colorex Salmonella - Prepared Plated Culture Media
Colorex™ Salmonella allows for simultaneous growth, detection and chromogenic differentiation of Salmonella species, including S. typhi and S. paratyphi, traditionally taken from clinical stool specimens. Additionally, Colorex Salmonella inhibits the growth of yeasts, mold and fungi – resulting in 100% sensitivity and 89% specificity for Salmonella compared to 78% with traditional Hektoen Agar.
Biomed - Model SARS-CoV-2 - Saline Solution
The Saline Solution (0.85%) is an isotonic solution, manufactured in compliance with ISO 13485:2016 standards. It is intended to be inoculated with nasopharyngeal (NP) or oropharyngeal (OP) synthetic fiber swab specimens (Not provided, see IFU for details), to be analyzed in the laboratory with validated qRT-PCR assays. This Saline Solution (0.85%) has been validated for the detection of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that causes COVID-19 disease in humans.1,2 The use of this device for other viral specimens is the responsibility of the end user including the validation thereof.
