*Aptima® CV/TV assays is not available in Canada at this time. Please check with your sales rep. Establishing a new standard for diagnosing vaginitis 4,5. The Aptima BV and Aptima CV/TV assays are indicated for use in symptomatic women to aid in the detection of BV, Candida species, Candida glabrata, and Trichomonas vaginalis on the Panther ...
Aptima Multitest Swab Specimen Collection Kit. Hold the swab, placing thumb and forefinger in the middle of the shaft covering the black score line. Do not hold the shaft below the score line. Carefully insert the swab into the vagina about 2 inches (5 cm) past the introitus and gently rotate the swab for 10 to 30 seconds. Make sure the swab
The Aptima Trichomonas vaginalis assay was first to market as an FDA-cleared and CE-marked nucleic acid amplification test (NAAT) for the qualitative detection of Trichomonas vaginalis.CDC guidelines recommend NAAT for detecting Trichomonas vaginalis over less sensitive methods such as wet-mount microscopy. 8 Available on the fully automated Panther system, the Aptima Trichomonas vaginalis ...
Aptima: Moving Humans, Technology, and AI Forward AI changes how we work, learn, and perform. Engineering Human-AI Teams. As workplaces evolve into multi-species organizations combining humans, agents, and AI, Aptima’s world-class multidisciplinary staff is addressing the distinct dynamics and challenges of integrating humans and AI systems.
For 25 years, Aptima’s mission has been to improve and optimize performance in mission-critical, technology-intensive settings. We apply deep expertise in how humans think, learn, and perform to today’s challenges. Whether for fighter pilots functioning in the cockpit, medical staff in the ICU, or teams collaborating across distributed ...
Aptima HPV Assay 2 AW-12820 Rev. 001 Aptima® General Information – Tigris DTS System and Panther System Intended Use The Aptima HPV assay is an in vitro nucleic acid amplification test for the qualitative detection of E6/E7 viral messenger RNA (mRNA) from 14 high-risk types of human papillomavirus (HPV) in cervical specimens.
Aptima Specimen Transfer Kit Aptima Specimen Transfer Kit 1 AW-15640 Rev. 004 Aptima® For in vitro diagnostic use. Intended Use The Aptima Specimen Transfer Kit consis ts of transfer tubes containing specimen transport medium (STM) and is intended for use with Aptima assays for the testing of gynecological specimens collected in ThinPrep Pap Test