System, Microbial Growth Monitor Of Normally Sterile Body Fluid Culture

Network appliance used in system

Single disposable - no packaging

Case with 256 cartridges.

Disposable used in system

NeuN, control

Neurofilament Control

HER-2 neu, Control

Beta-Catenin, Control

Cytokeratin 8&18, Control

Cytokeratin LMW CAM5.2, Control

p21, Control

Parathyroid Hormone/ PTH, Control

PGP 9.5, Control

PMS2 Control

Progesterone Receptor, Control

PSA, Control

S100 Beta, Control

Survivin, Control

Synaptophysin, Control

TdT, Control

PCRopsis™ Universal Viral Transport is intended for the collection and non-propagating transport of clinical specimens containing viruses, chlamydiae, mycoplasmas or ureaplasmas from the collection site to the testing laboratory.

PCRopsis™ Universal Viral Transport is intended for the collection and non-propagating transport of clinical specimens containing viruses, chlamydiae, mycoplasmas or ureaplasmas from the collection site to the testing laboratory.

PCRopsis™ Universal Viral Transport is intended for the collection and non-propagating transport of clinical specimens containing viruses, chlamydiae, mycoplasmas or ureaplasmas from the collection site to the testing laboratory.

PCRopsis™ Universal Viral Transport (UVT) is intended for the collection and non-propagating transport of clinical specimens containing viruses, chlamydiae, mycoplasmas or ureaplasmas from the collection site to the testing laboratory. PCRopsis™ UVT (3 mL) is aliquoted into 100x sterile, 10 mL transport tubes.

PCRopsis™ Universal Viral Transport (UVT) is intended for the collection and non-propagating transport of clinical specimens containing viruses, chlamydiae, mycoplasmas or ureaplasmas from the collection site to the testing laboratory. PCRopsis™ UVT (1.5 mL) is aliquoted into 100x sterile, 10 mL transport tubes.

The iCubate, Inc. iC-GPC Assay for use on the iC-System is a qualitative, multiplexed, in vitro diagnostic test for the detection and identification of potentially pathogenic gram positive bacteria, which may cause bloodstream infection (BSI). The iC-GPC Assay is performed directly on positive blood cultures, confirmed by Gram stain to contain gram positive cocci.

The iCubate, Inc. iC-GN Assay for use on the iC-System is a qualitative, multiplexed, in vitro diagnostic test for the detection and identification of potentially pathogenic gram negative bacteria, which may cause bloodstream infection (BSI). The iC-GN Assay is performed directly on positive blood cultures, confirmed by Gram stain to contain gram negative bacilli.

The Accula Dock is an electronic module which executes in vitro diagnostic tests on compatible Test Cassettes. It consists of anelectro-mechanical interface to a single Test Cassette. The Dock contains all electrical systems, controls and logic necessary toorchestrate in-vitro diagnostic tests within the inserted Test Cassette.

The Programming Cassette is an accessory to the Accula Dock and facilitates reprogramming of the Dock’s embedded firmware. When firmware updates are needed, the firmware will be stored onto Programming Cassettes and sent to end users, who will load the Programming Cassette into their Dock and re-program its firmware

The Accula™ Flu A / B Test performed on the Accula Dock is a molecular in vitro diagnostic test utilizing polymerasechain reaction (PCR) and lateral flow technology for the qualitative, visual detection and differentiation of influenza A andinfluenza B viral RNA. The Accula Flu A / B Test uses a nasal swab specimen collected from patients with signs andsymptoms of respiratory infection. Accula Flu A / B assay is intended as an aid in the diagnosis of influenza infectionsin conjunction with clinical and epidemiological risk factors. The assay is not intended to detect the presence of influenzaC virus.

The Accula™ Flu A / B Control Kit is intended for in vitro diagnostic use in qualitycontrol testing with the Accula™ Flu A / B Test.

Dorsal Lapidus Guide, Left, 28mm x 23mm

Immunochromatographic test kit for presumptive identification of Bacillus anthracis colonies

Westernblot-assay for the detection of IgG antibodies against Borrelia burgdorferi s.s. / B31 im human serum.

Westernblot-assay for the detection of IgM antibodies against Borrelia burgdorferi s.s. / B31 im human serum.

Immunoassay for the detection of IgG antibodies against Borrelia burgdorferi s.s. / B31 in human serum.

Immunoassay for the detection of IgG antibodies against Borrelia burgdorferi s.s. / B31 in human serum.

Immunoassay for the detection of IgM antibodies against Borrelia burgdorferi s.s. / B31 im human serum.

Immunoassay for the detection of IgM antibodies against Borrelia burgdorferi s.s. / B31 in human serum.

Immunoassay for the detection of IgG antibodies against Borrelia burgdorferi s.s. / B31 im human serum.

Immunoassay for the detection of IgG antibodies against Borrelia burgdorferi s.s. / B31 im human serum.

Immunoassay for the detection of IgG antibodies against Borrelia burgdorferi s.s. / B31 in human serum.

Immunoassay for the detection of IgM antibodies against Borrelia burgdorferi s.s. / B31 im human serum.

Immunoassay for the detection of IgM antibodies against Borrelia burgdorferi s.s. / B31 im human serum.

Immunoassay for the detection of IgM antibodies against Borrelia burgdorferi s.s. / B31 im human serum.

Immunoassay for the detection of antibodies against Borrelia sp. in human serum.

Immunoassay for the detection of antibodies against Borrelia sp. in human serum.