A sterile, wireless, battery operated probe used to detect and quantify gamma rays from Tc-99m and I-125 isotopes, communicated to the User Feedback Unit.

The OMNI™ Hysteroscope is used to provide viewing of the cervical canal and the uterine cavity for the purpose of performing diagnostic and surgical procedures.

The OMNI™Hysteroscope is used to provide viewing of the cervical canal and the uterine cavity for the purpose of performing diagnostic and surgical procedures.

I-View

Aptima® BV assay, 100 test, box 1 of 2 (2°C to 8°C box). The Aptima® BV assay is an in vitro nucleic acid amplification test that utilizes real time transcription-mediated amplification (TMA®) for detection and quantitation of ribosomal RNA from bacteria associated with bacterial vaginosis (BV), including Lactobacillus (L. gasseri, L. crispatus, and L. jensenii), Gardnerella vaginalis, and Atopobium vaginae.

Aptima® BV assay, 100 test, box 2 of 2 (15°C to 30°C box). The Aptima® BV assay is an in vitro nucleic acid amplification test that utilizes real time transcription-mediated amplification (TMA®) for detection and quantitation of ribosomal RNA from bacteria associated with bacterial vaginosis (BV), including Lactobacillus (L. gasseri, L. crispatus, and L. jensenii), Gardnerella vaginalis, and Atopobium vaginae.

Aptima® CV/TV assay, 100 test, box 1 of 2 (2°C to 8°C box). The Aptima® CV/TV assay is an in vitro nucleic acid amplification test for the detection of RNA from microorganisms associated with vulvovaginal candidiasis and trichomoniasis.

Aptima® CV/TV assay, 100 test, box 2 of 2 (15°C to 30°C box). The Aptima® CV/TV assay is an in vitro nucleic acid amplification test for the detection of RNA from microorganisms associated with vulvovaginal candidiasis and trichomoniasis.

Selenia® Dimensions® compression paddles provide an optically and radiographically transparent surface to immobolize and flatten the patient breast, ensuring the highest possible image quality with minimum patient discomfort.

Selenia® Dimensions® compression paddles provide an optically and radiographically transparent surface to immobolize and flatten the patient breast, ensuring the highest possible image quality with minimum patient discomfort.

Selenia® Dimensions® compression paddles provide an optically and radiographically transparent surface to immobolize and flatten the patient breast, ensuring the highest possible image quality with minimum patient discomfort.

Computer to operate the ThinPrep® Imager DUO System.

Aptima Combo 2® Assay, 250 test, box 2 of 2 (15°C to 30°C box). The Aptima Combo 2® assay is a target amplification nucleic acid probe test that utilizes target capture for the in vitro qualitative detection and differentiation of ribosomal RNA (rRNA) from Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) to aid in the diagnosis of chlamydial and/or gonococcal urogenital disease.

Aptima Combo 2® Assay, 250 test, box 1 of 2 (2°C to 8°C box). The Aptima Combo 2® assay is a target amplification nucleic acid probe test that utilizes target capture for the in vitro qualitative detection and differentiation of ribosomal RNA (rRNA) from Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) to aid in the diagnosis of chlamydial and/or gonococcal urogenital disease.

Aptima Combo 2® Assay, 100 test, box 2 of 2 (15°C to 30°C box). The Aptima Combo 2® assay is a target amplification nucleic acid probe test that utilizes target capture for the in vitro qualitative detection and differentiation of ribosomal RNA (rRNA) fromChlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) to aid in the diagnosis of chlamydial and/or gonococcal disease using the Panther® system as specified.

Aptima Combo 2® assay, 100 test, box 1 of 2 (2°C to 8°C box). The Aptima Combo 2® assay is a target amplification nucleic acid probe test that utilizes target capture for the in vitro qualitative detection and differentiation of ribosomal RNA (rRNA) from Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) to aid in the diagnosis of chlamydial and/or gonococcal disease using the Panther® system as specified.

Contrast Enhanced Digital Mammography Imaging Kit

Genius AI® is a computer-aided detection and diagnosis (CADe/CADx) software device intended to be used with compatible digital breast tomosynthsis (DBT) systems to identify and mark regions of interest including soft tissue densities (masses, architectural distortions, and assymetries) and calcifications in DBT exams from compatible DBT systems and provide confidence scores that offer assessment for Certainty of Findings and a Case Score.

Single-use, disposable needle for acquiring biopsy specimens.

Computer to operate the ThinPrep® Imaging System.

Affirm® breast biopsy guidance system software is designed to allow the accurate location of lesions in the breast in three dimensions. It is intended to provide guidance for interventional purposes such as biopsy, pre-surgerical localization or treatment devices.

Panther Fusion® Internal Control-X.

Panther Fusion® Extraction Reagent-X.

The Panther Fusion® GBS assay is an automated qualitative in vitro diagnostic test utilizing realtime PCR for detection of Group B Streptococcus DNA.

Panther Fusion® GBS Controls Kit.

Processes Non Gyn specimens to produce a uniform layer of cells on a glass microsope slide. It can also remove an aliquot from a specimen preserved in PreservCyt®.

Aptima® BV Assay Controls Kit.

Aptima® BV Assay Calibrator.

Aptima® CV/TV Assay Controls Kit.

Aptima® CV/TV Assay Calibrator.

Coronavirus (CoV) HKU1 Primers ASR.

Coronavirus (CoV) HKU1 Probe ASR.

Coronavirus (CoV) OC43 Primers ASR.

Coronavirus (CoV) OC43 Probe ASR.

Coronavirus (CoV) 229E Primers ASR.

Coronavirus (CoV) 229E Probe ASR.

Coronavirus (CoV) NL63 Primers ASR.

Coronavirus (CoV) NL63 Probe ASR.

Panther Fusion® Extraction Reagents-B.

Panther Fusion® Internal Control-B.

Cabinet x-ray device used to generate x-ray of specimens from various anatomical regions

Unifi® Software is a software application that is intended for use in receiving, processing, manipulating, displaying, printing, and archiving mammmography images as well as other medical images and data.

Unifi® Software is a software application that is intended for use in receiving, processing, manipulating, displaying, printing, and archiving mammmography images as well as other medical images and data.