The BacT/ALERT 3D Combination contains an integrated Control and Incubator Module with two right hand configured 60 capacity drawers for a total combined capacity of 120 cells.

The BacT/ALERT 3D Combination contains an integrated Control and Incubator Module with two left hand configured 60 capacity drawers for a total combined capacity of 120 cells.

The BacT/ALERT 3D Control Module enables up to 6 incubator modules to be operated from one integrated touchscreen computer.

the BacT/ALERT 3D Left Incubator Module has four independent drawers of 60 cells each. Patented cell flags track bottle movements between cells for greater ease of use.

The BacT/ALERT 3D Right Incubator Module has four independent drawers of 60 cells each. Patented cell flags track bottle movements between cells for greater ease of use.

VITEK 2 Pipettor / Diluter Accessory Kit containing straws for VITEK 2 and VITEK 2 XL needed to prepare sample suspensions.

API® Listeria is a standardized system for the identification of Listeria, which uses miniaturized tests, as well as a database

API® NH is for ID of Neisseria, Haemophilus (and related genera) and Moraxella catarrhalis (Branhamella catarrhalis).

API 20 NE is a standardized system for the ID of non-fastidious, non-enteric Gram-negative rods (e.g. Pseudomonas, Acinetobacter, Flavobacterium, Moraxella, etc.)

API 20 C AUX is a system for the precise identification of the most frequently encountered yeasts.

The API 20 A system enables 21 tests to be carried out for ID of anaerobes. Other tests such as colonial and microscopic morphology, Gram stain, etc. to confirm or complete ID

API® Staph is a standardized system for the identification of the genera Staphylococcus, Micrococcus and Kocuria

API 20 Strep combines 20 biochemical tests to enable group or species ID of most streptococci and enterococci

API Campy is a standardized system for the identification of Campylobacter.

API Coryne is a standardized system for the identification of coryneform bacteria in 24 hours

VIDAS VARICEL. ZOSTER IGG assay is a quantitative IA intended for use on VIDAS family instrument in the detection of IgG antibodies to Varicella Zoster in human serum.

VIDAS Mumps IgG (MPG) is qualitative test for use on s VIDAS family instruments for the detection of IgG antibodies to mumps virus

VIDAS Measles IgG (MSG) assay is a quantitative IA intended for use on VIDAS family instrument in the detection of IgG antibodies to measles (rubeola) in human serum.

ID 32 C is a standardized system for the identification of yeasts, which uses 32 miniaturized assimilation tests and a database.

Trypcase Soy broth is a culture medium for the growth of most non-fastidious micro-organisms (bacteria and fungi)

Reagent associated to all API references except API LISTERIA (10 300) 1 API ZYM (25 200) to close the cupule to the atmosphere

TDA is a reagent associated to API 20 E (20 100/20 160), API® 10 S (10 100)

VP1 VP2 are reagents associated to API 20 E™ (20 100/20 160), RapiD 20 E™ (20 701), API® Staph (20 500), API® 20 Strep (20 600)

Reagents associated to API 20 E™ (20 100/20 160), API® 10 S (10 100), API® 20 NE (20 050), API® Staph (20 500), API® Coryne (20 900), API® Campy (20 800), ID 32 STAPH (32 500), rapid ID 32 A (32 300)

BCP is a reagent associated to API 20 A® (20 300) & rapid ID 32 E (32 700)

EHR is a reagent associated to API 20 A® (20 300)

JAMES is a reagent associated to API® NH, API 20 ETM, API® 10 S, RapiD 20 ETM, API® 20 NE, RAPIDEC® ur, ID 32 E), rapid ID 32 A, rapid ID 32 E

FB is a reagent associated to API® Campy (20 800), ID 32 STAPH (32 500), rapid ID 32 A (32 300), rapid ID 32 STREP (32 600)

VPA VPB is a reagent associated to ID 32 STAPH (32 500) & rapid ID 32 STREP (32 600)

McFarland Standard is a series of standards of different opacity, allowing the estimation of the density of bacterial suspensions.

ETEST® is a manual, quantitative technique for determination of antimicrobial susceptibility of non-fastidious Gram-negative and Gram-positive aerobic bacteria and fastidious bacteria.

Detection in enterobacteria of indole production and the presence of a tryptophan deaminase (TDA). It allows presumptive differentiation of bacteria possessing these characteristics

selective enrichment broth for the detection of group B streptococci in pregnant women.

AccuDiag™ Cytomegalovirus IgM ELISAA collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of immunoglobulin M (IgM) antibodies to cytomegalovirus (CMV) in a clinical specimen, using an enzyme immunoassay (EIA) method.

AccuDiag™Measles IgM ELISA KitA collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of immunoglobulin M (IgM) antibodies to Measles virus in a clinical specimen, using an enzyme immunoassay (EIA) method.

ASO Latex Test Kit:Diagnostic Automation Inc. Latex agglutination slide test for the Qualitative and Semi-quantitative determination of Antistreptolysin-O in non-diluted serum.

AccuDiag ™ Toxocara IgG ELISAThe Toxocara ELISA test is a qualitative enzyme immunoassay for the detection of antibodies to Toxocara, in samples of human serum or plasma.

AccuDiag ™ Strongyloides IgG ELISAThe Strongyloides ELISA test is a qualitative enzyme immunoassay for the detection of antibodies to Strongyloides, in samples of human serum or plasma.

The DA50TS8 Microplate Washer is a compact microplate washing system with functionality that is unsurpassed in its class. The 4.3” color LCD touchscreen provides a visual interface with menu-driven programming that makes creating protocols fast and intuitive. The DAW50TS is an affordable choice for automating the wash steps of a variety of applications in clinical and research laboratories. Used in conjunction with the DAR800TS Absorbance Reader or other detection systems, the DAW50TS offers a welcome upgrade from manual processing - bringing convenience and consistently high-quality results to your laboratory’s plate washing workflows.

An in vitro diagnostic test for the detection of malaria HRP2 (histidine-rich protein 2) of Plasmodium falciparum and pLDH (Plasmodium lactate dehydrogenase) of Plasmodium vivax in human whole blood as an aid in the diagnosis of malaria infection.

An in vitro diagnostic test for the detection of Dengue NS1 protein in human whole blood of dengue infected patient from acute to convalescent stage.

An in vitro diagnostic test for the detection of influenza A and influenza B viral nucleoprotein antigens from nasopharyngeal secretion specimens in symptomatic patients.

QuantStudio Real-Time PCR Instrument Qualified by OpGen for use with Acuitas AMR Gene Panel.

QIAGEN EZ1 Advanced XL Instrument for use with Acuitas AMR Gene Panel.

Labeled, OpGen branded flash drive containing IVD Acuitas AMR Gene Analysis Software.

PCR Assay Plate Kit for use with Acuitas AMR Gene Panel assay; consisting of two (2) PCR Assay Plates and one (1) PCR Plate Seal Package in a labeled, white, reverse tuck box.

A reagent kit for use with Acuitas AMR Gene Panel assay; consisting of two (2) vials of PCR Master Mix and eight (8) vials of dried Assay Control which comprise enough reagents required to perform eight (8) Acuitas AMR Gene Panel assays.

NATtrol™ BV Negative Control (NATBVNEG-BD) is intended for use as an assayed quality control material to monitor the performance of in vitro diagnostic laboratory nucleic acid testing procedures for the qualitative detection of targets on the BD Vaginal Panel for the BD MAX™ System. NATtrol BV Negative Control is a qualitative control containing intact and inactivated Lactobacillus crispatus and intended to be used solely with the BD Vaginal Panel for BD MAX™ System. This product is not intended to replace manufacturer controls provided in the package insert.

NATtrol™ BV Positive Control (NATBVPOS-BD) is intended for use as an assayed quality control material to monitor the performance of in vitro diagnostic laboratory nucleic acid testing procedures for the qualitative detection of targets on the BD Vaginal Panel for the BD MAX™ System. NATtrol™ BV Positive Control is a qualitative control containing intact and inactivated Lactobacillus jensenii, Gardnerella vaginalis, Atopobium vaginae, and Saccharomyces cerevisiae containing BVAB2 (Bacterial Vaginosis-Associated Bacterium 2) sequence and intended to be used solely with the BD Vaginal Panel for BD MAX™ System. This product is not intended to replace manufacturer controls provided in the package insert.

NATtrol™ Candida/TV Positive Control (NATCTVPOS-BD) is intended for use as an assayed quality control material to monitor the performance of in vitro diagnostic laboratory nucleic acid testing procedures for the qualitative detection of targets on the BD Vaginal Panel for BD MAX™ System. NATtrol Candida/TV Positive Control is a qualitative control containing intact and inactivated Candida albicans, Candida krusei, Candida glabrata, and Trichomonas vaginalis and intended to be used solely with the BD Vaginal Panel for the BD MAX™ System. This product is not intended to replace manufacturer controls provided in the package insert.