Count on high-quality Abbott™ diagnostic products and services for reliable and actionable information to help providers improve patient care. Through the use of innovative technologies, we not only transform diagnostic products, but also expand into new platforms and solutions, resulting in better clinical and economic outcomes.

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Now CLIA Waived

Abbott i Influenza A and B Test Kit

Highly accurate, molecular results in less than 15 minutes. Rapid diagnosis of influenza can lead to reduced hospital stays, secondary complications, and cost of hospital care.1,2

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Abbott i Influenza A and B Control Swab Kit

Includes 20 nasal swabs for the detection of influenza A and B.

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Determine HIV-1/2 Ag/Ab Combo
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Earlier HIV Detection

Abbott Determine HIV-1/2 Ag/Ab Combo Test 

Abbott™ Determine™ HIV-1/2 Ag/Ab Combo is a fourth-generation test that has the ability to detect HIV earlier than second- and third-generation antibody-only tests.2 It can detect infection three weeks after it occurs as opposed to other tests that can only detect it after three months. This enables healthcare providers to diagnose HIV infection earlier, allowing individuals to seek medical care sooner.

Features include:

  • CLIA waived for fingerstick whole blood
  • Requires minimal training
  • Test in three easy steps
  • Receive results in just 20 minutes
  • Test using whole blood, serum, or plasma
  • Proven 99.9% overall clinical sensitivity for all sample types

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Breaking the HIV Infection Cycle

Identifying HIV infection early, during the most infectious stage, offers significant benefits, particularly in high-risk populations such as men who have sex with men and injecting drug users.

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Rapid detection also helps get patients into effective care and treatment earlier.

Individuals who are unaware of their infection are 3.5 times more likely to transmit the virus to someone else.1

By detecting HIV earlier, further transmission can be prevented during this highly infectious stage.

Shiga Toxin Quik Chek
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Diagnose Sooner with Results in 30 Minutes

Abbott Shiga Toxin Quik Chek

The new Abbott™ Shiga Toxin Quik Chek™ assay is the only rapid test able to detect shiga toxin-producing E. Coli (STEC) toxins directly from fecal samples. The assay simultaneously detects and differentiates Stx1 and Stx2 toxins from STEC.

Unique Product

  • Direct detection of STEC toxins from primary fecal samples
  • Diagnosis up to 24 hours earlier than other rapid tests or traditional methods
  • Analytical Sensitivity: 0.04ng/mL Stx1 and Stx2
  • Differentiation of shiga toxins (Stx1 and Stx2)

Easy to Use

  • Utilizes the popular Techlab, Inc. QUIK CHEK format
  • Results in under 30 minutes
  • Compatible with primary fecal samples, broth, plate cultures, and specimens in transport media
 

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C. Diff Quik Chek Complete
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Confirm if It's C. Diff  in 30 Minutes

Abbott C. Diff  Quik Chek Complete

The Abbott™ C. Diff Quik Chek Complete™ test is the only rapid cassette assay that simultaneously detects both glutamate dehydrogenase (GDH) antigen and toxins A & B of C. difficile in fecal specimens. The test detects C. difficile antigen, GDH, as a screen for the presence of C. difficile and confirms the presence of toxigenic C. difficile by detecting toxins A and B in fecal specimens from persons suspected of having C. difficile disease.

Benefits

  • Accurate: The C. Diff Quik Chek Complete test provides a final answer for up to 90% of samples in one test
  • Rapid: The test yields results in less than 30 minutes
  • Flexible: Samples may be performed in batches or individually for on-demand testing
  • Convenient: The test works with any specimen consistency and with samples stored in transport media such as Cary Blair or C&S

Specifications

  • The antigen portion of the C. Diff Quik Chek Complete Test detected 98.7% of the cyto-toxicity tissue culture-positive samples
  • The negative predictive value for the toxin portion compared to cyto-toxicity tissue culture was 98.1%
  • Toxin sensitivity was 87.8% compared to cyto-toxicity tissue culture
  • Toxin specificity was 99.4% compared to cyto-toxicity tissue culture
  • Kit sizes = 25 tests or 50 tests
 

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References 

1.  Williams, KM, Jackson MA, Hamilton M. (2002) Rapid Diagnostic Testing for URIs in Children: Impact on Physician Decision Making and Cost. Infect. Med. 19(3): 109-111.

2.   Bonner, A.B. et al. (2003) Impact of the Rapid Diagnosis of Influenza on Physician Decision-Making and Patient Management in the Pediatric Emergency Department: Results of a Randomized, Prospective, Controlled Trial. Pediatrics. Vol. 112 No. 2.