VITEK ® 2 software 8.01 update, advanced software to run your VITEK ® 2 system

VITEK®2 software 9.01.0, advanced software to run your VITEK®2 system

Mycobacteria Detection bottle for recovery and detection of mycobacteria from sterile body specimens other than blood, and from digested-decontaminated clinical specimens.

BacT/ALERT BPA (aerobic culture) bottles are used for QC testing of leukocyte reduced apheresis platelet units,leukocyte reduced single units of whole blood platelet concentrates

BacT/ALERT BPN (anaerobic culture) bottles: used for QC testing of leukocyte reduced apheresis platelet units,leukocyte reduced single units of whole blood platelet concentrates.

The BACT/ALERT FA Culture Bottles are used for enhanced recovery and detection of aerobic and facultative anaerobic microorganisms from blood, other normally sterile body fluids.

The BACT/ALERT FA Plus Culture Bottles are used for the recovery and detection of aerobic microorganisms (bacteria and fungi) from blood and other normally sterile body fluids.

The BACT/ALERT FN Culture Bottles are used for enhanced recovery and detection of anaerobic microorganisms from blood, and other normally sterile body fluids.

The BACT/ALERT FN Plus Culture Bottles are used for the recovery and detection of anaerobic,facultative anaerobic microorganisms from blood and other normally sterile body fluids

BACT/ALERT® PF Culture Bottles are used in qualitative procedures for recovery and detection of aerobic and facultative anaerobic microorganisms (bacteria and yeast) from blood

The BACT/ALERT PF Plus Culture Bottles are used for recovery and detection of aerobic and facultative anaerobic microorganisms (bacteria and yeast) from blood.

The BACT/ALERT SA Culture Bottles are used for the recovery and detection of aerobic microorganisms (bacteria and fungi) from blood and other normally sterile body fluids.

The BACT/ALERT SN Culture Bottles are used for the recovery and detection of anaerobic and facultative anaerobic microorganisms from blood and other normally sterile body fluids.

These are calibration standards for the DensiCHEK™ Plus instrument which is designed for use with the VITEK®2 to measure the optical density of a bacterial suspension.

VITEK 2.0 0.45% SALINE INDIVIDUAL BAG

VITEK® 2 Gram Negative Susceptibility Card is intended for use with the VITEK 2 Systems to determine the susceptibility of clinically significant aerobic gramnegative bacilli

VITEK ® 2 Gram Positive Susceptibility Card is intended for use with the VITEK 2 to determine the susceptibility of Staphylococcus spp., Enterococcus spp., and S. agalactiae

The VITEK® 2 Streptococcus Susceptibility Card is intended for use with the VITEK 2 Systems to determine the susceptibility of S. pneumoniae, beta-hemolytic Streptococcus, and Viridans Streptococcus

VITEK® 2 Gram Negative Susceptibility Card is intended for use with the VITEK 2 Systems to determine the susceptibility of clinically significant aerobic gram-negative bacilli

API 20 E is a standardized identification system for Enterobacteriaceae and other non-fastidious, Gramnegative rods

API 20 E Reagent QC test kit is a abbreviated version of API 20 E strip containing substrates for tryptophane deaminase, indole, nitrate reduction and Voges-Proskauer tests

API 50 CH combines 50 biochemical tests for ID of Lactobacillus and related genera as well as Bacillus and related genera, Enterobacteriaceae and Vibrionaceae.

API 50 CHB/E Medium is for ID of Bacillus, related genera, and GN rods (Enterobacteriaceae and Vibrionaceae). It allows fermentation of 49 carbohydrates on API 50 CH strip

API 50 CHL Medium, for ID of Lactobacillus and related genera, is a ready-to-use allowing fermentation of the 49 carbohydrates on the API 50 CH strip (Ref. 50 300).

Manual reagent for catalase test. API®strips give accurate identifications based on extensive databases and are standardized, easy-to-use test systems.

API M Medium allows the differentiation between motile and non-motile bacteria of the facultative aero-anaerobic group. It can be used to complement the API 20 E strip.

NaCl 0.85 % Medium and Suspension Medium are designed to be used as suspension media with API ®, ID 32 or ATB™ products.

NaCl 0.85 % Medium and Suspension Medium are designed to be used as suspension media with API ®, ID 32 or ATB™ products.

NaCl 0.85 % Medium and Suspension Medium are designed to be used as suspension media with API ®, ID 32 or ATB™ products.

API ® OF Medium enables lab personnel to differentiate oxidative or fermentative metabolism of glucose by bacteria. It is designed to be used with API 20 E strips.

NaCl 0.85 % Medium and Suspension Medium are designed to be used as suspension media with API®, ID 32 or ATB™ products, in the conditions defined in the package inserts of these products

Chromogenic medium for the screening and qualitative detection of methicillin-resistant Staphylococcus aureus (MRSA)

Chromogenic medium for the screening and qualitative detection of methicillin-resistant Staphylococcus aureus and selective isolation of staphylococci and the direct identification of S. aureus.

Chromogenic medium for the qualitative detection of Enterococcus faecium and E. faecalis showing acquired vancomycin resistance (VRE) in stool specimens.

Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.

Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.

Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.

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

Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.

Selective isolation of Escherichia coli O157 :H7, and, for industrial applications only, enterohemorrhagic E. coli

ID 32 STAPH is a standardized system for the identification of the genera Staphylococcus, Micrococcus and related genera, Rothia and Aerococcus

4-hour ID of Enterobacteriaceae. API®strips give accurate ID based on extensive databases and are standardized, easy-to-use test systems.

rapid ID 32 A is a standardized system for the identification of anaerobes in 4 hours

rapid ID 32 E is a standardized system for the identification of Enterobacteriaceae in 4 hours

rapid ID 32 STREP is a standardized system for the identification of streptococci and enterococci, and those most common related organisms, in 4 hours

The VITEK MS-CHCA matrix is used with the VITEK® MS System to enable identification of microorganisms. The matrix absorbs energy from the VITEK MS laser and transfers it to the microorganisms

VITEK ® MS - FA is used to pretreat yeasts to facilitate their identification according to the MALDI - TOF method. It is used exclusively with the VITEK ® MS instrument.

The VITEK MS-DS target slides enable the identification of microorganisms according to the MALDI-TOF mass spectrometry method.

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

Zn is a reagent associated to API 20 E® (20 100) API 20 NE® (20 050) API 50 CH® (50 300) API 50 CHB/E® (50 430)