Biotyper system for clinical use in the USA.

Reuseable Stainless Steel Target.

Biotyper system for clinical use in the USA, for Becton Dickinson.

Biotyper system for clinical use in the USA, with smart laser.

Biotyper system for clinical use in the USA with smart laser, for Becton Dickson.

Lyme B. burgdorferi (IgG) Marstripe Test

Lyme B. burgdorferi (IgG) Marstripe Test

Lyme B. burgdorferi (IgG) Marstripe Test

Lyme B. burgdorferi (IgM) Marstripe Test

Lyme B. burgdorferi (IgM) Marstripe Test

Lyme B. burgdorferi (IgM) Marstripe Test

Para-Pak systems are convenient systems for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites. It is designed for easy use by individuals not trained in microbiological techniques and affords an excellent means of minimizing the adverse effects of delay in specimen transport.

Para-Pak systems are convenient systems for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites. It is designed for easy use by individuals not trained in microbiological techniques and affords an excellent means of minimizing the adverse effects of delay in specimen transport.

Para-Pak systems provide standardized procedures for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites. Systems are designed for easy use by individuals not trained in microbiological procedures and afford an excellent means of minimizing the adverse effects of delay in specimen transportation.

Para-Pak systems provide standardized procedures for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites. Systems are designed for easy use by individuals not trained in microbiological procedures and afford an excellent means of minimizing the adverse effects of delay in specimen transportation

Para-Pak systems are systems for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites. It is designed for easy use by individuals not trained in microbiological techniques and affords an excellent means of minimizing the adverse effects of delay in specimen transportation.

Para-Pak systems are systems for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites. It is designed for easy use by individuals not trained in microbiological techniques and affords an excellent means of minimizing the adverse effects of delay in specimen transportation.

Para-Pak systems provide standardized procedures for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites. Systems are designed for easy use by individuals not trained in microbiological procedures and afford an excellent means of minimizing the adverse effects of delay in specimen transportation.

Para-Pak systems provide standardized procedures for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites. Systems are designed for easy use by individuals not trained in microbiological procedures and afford an excellent means of minimizing the adverse effects of delay in specimen transportation.

The Para-Pak system is a convenient system for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites / bacterial pathogens. It is designed for easy collection of specimens by individuals not trained in microbiological techniques and affords an excellent means of minimizing the adverse effects of delay in specimen transportation.

The Para-Pak system is a convenient system for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites / bacterial pathogens. It is designed for easy collection of specimens by individuals not trained in microbiological techniques and affords an excellent means of minimizing the adverse effects of delay in specimen transportation.

Para-Pak systems are convenient system for the routine collection, transportation, preservation and examination of stool specimens for intestinal parasites. The systems are designed for easy collection of specimens by individuals not trained in microbiological techniques and affords and excellent means of minimizing the adverse effects of delay in specimen transport.

Para-Pak systems are convenient system for the routine collection, transportation, preservation and examination of stool specimens for intestinal parasites. The systems are designed for easy collection of specimens by individuals not trained in microbiological techniques and affords and excellent means of minimizing the adverse effects of delay in specimen transport.

Para-Pak and Para-Pak Ultra based systems provide standardized procedures for the routine collection, transportation, preservation and examination of stool specimens for intestinal parasites. Kit systems are designed for easy use by individuals not trained in microbiological procedures and afford an excellent means of minimizing the adverse effects of delay in specimen transportation. Bulk products for preservation of fresh specimens are also available.

Para-Pak and Para-Pak Ultra systems provide standardized procedures for the routine collection, transportation, preservation and examination of stool specimens for intestinal parasites. Kit systems are designed for easy use by individuals not trained in microbiological procedures and afford an excellent means of minimizing the adverse effects of delay in specimen transportation. Bulk products, for preservation of fresh specimens are also available.

The Para-Pak C&S (Culture and Sensitivity) and Para-Pak Enteric Plus provide a standardized procedure for the routine collection, transportation, preservation, and culture of stool specimens for bacterial enteric pathogens. It is designed for easy collection of specimens by individuals not trained in microbiological techniques and affords an excellent means of minimizing the adverse effects of delay in specimen transportation.

The Meridian CON-Trate System is a complete system for concentrating and recovering helminth eggs, larvae and protozoan cysts from feces.

The MERIFLUOR EBV-EA IgG IFA Test is a sensitive and rapid immunofluorescence method for the qualitative and quantitative detection of antibodies to early antigen (EA) of Epstein-Barr virus (EBV) in human serum. When performed according to instructions, the MERIFLUOR EBV-EA IgG IFA Test detects IgG antibodies to the diffuse (D) and restricted (R) components of the EBV-EA complex. It is of value in providing supportive information for the diagnosis of EBV associated disease.

STAND,INPUT BOX/PHOTIC EEG-1200

M4RT(3ml) Dual Swab KIT

M4RT(3ml) 2NPG Swab KIT

M4RT (3ml) no BEADS Nasal Swab Kit w/bag

SPECTRA Strep A Agar 10/PK

Saline,0.85% (3ml) 100/PK

M4RT Tube PK/72

M4RT KIT w/ FLOCKED SWAB PK/100

M4RT(3ml) w/o beads PK/72

Herpes-1 IgG (HSV1) Atellica IM - RGT - 100T

Herpes-2 IgG (HSV2) Atellica IM - RGT - 100T

For the quantitative measurement of antistreptolysin O in human serum and plasma on the Dimension Vista® System

Determination of Anti-Streptotysin O (ASL) in human serum and plasma on BN II and BN ProSpec Systems

Determination of Anti-Streptotysin O (ASL) in human serum and plasma on BN II and BN ProSpec Systems

Qualitative detection or semi-quantitative determination of anti-streptolysin O (ASL) in human serum

Qualitative detection or semi-quantitative determination of anti-streptolysin O (ASL) in human serum

Qualitative detection or semi-quantitative determination of anti-streptolysin O (ASL) in human serum

Quantitative determination of ADNase B in human serum on BN Systems

MDx-Chex for BCID2 is intended for use as an external positive and negative assayed control to monitor the performance of the qualitative detection of yeast, Gram positive and Gram negative bacteria, as well as associated antimicrobial resistance genes, by the BioFire® FilmArray® Blood Culture Identification 2 (BCID2) Panel on FilmArray® systems. Control 1 - GN: Gram negative bacteria: Acinetobacter colcoaceticus-baumannii complex, Bacteroides fragilis, Enterobacter cloacae complex, Escherichia coli, Klebsiella aerogenes, Klebsiella oxytoca, Klebsiella pneumoniae group, Proteus spp., Salmonella spp., Serratia marcescens, Haemophilus influenza, Neisseria meningitides, Pseudomonas aeruginosa, Stenotrophomonas maltophilia; antimicrobial resistance genes: KPC, CTX-M, IMP, NDM, OXA-48-like, VIM, mcr-1. Control 2 - GPY: Gram positive bacteria: Enterococcus faecalis, Enterococcus faecium, Listeria monocytogenes, Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus lugdunesis, Streptococcus agalactiae, Streptococcus pneumonia, Streptococcus pyogenes; yeast: Candida albicans, Candida auris, Candida glabrata, Candida krusei, Candida parapsilosis, Candida tropicalis, Cryptococcus neoformans/gatti; antimicrobial resistance genes: mecA/C and MREJ, vanA/B. This product is not intended to replace manufacturer controls provided with the device.

The ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System is intended for the qualitative detection of IgG and IgM class antibodies to VlsE1 and pepC10 antigens from Borrelia burgdorferi in human serum. The assay is intended for testing serum samples from symptomatic patients or those with a history of Lyme Borreliosis. All positive and equivocal specimens should be tested with a second-tier test such as Western Blot, which if positive, is supportive evidence of infection with Borrelia burgdorferi. Diagnosis of Lyme Borreliosis should be made based on the presence of B. burgdorferi antibodies, history, symptoms, and other laboratory data. Negative first or second tier results should not be used to exclude Borreliosis. This assay is for In Vitro diagnostic use.