There are many office lab tests, or lab tests done remotely that do not need regulatory oversight, as long as the using party registers.  “Tests can be categorized as FDA “waived” from regulatory oversite if they meet certain requirements established by the Clinical Laboratory Improvement Amendments of 1988 (CLIA) law”.  Test such a HIV, cardiac enzymes, prothombin, CBSs, Electrolytes, Drug Screens, Alcohol levels, and many other provide an excellent Point of Care evaluation of all these lab test.  This technology will eventually spread to big clinics, and emergency rooms, so that, not only are lab test results obtained quicker, but the overall lab tests cost will be decreased greatly.

ClearView HIV 1/2 Stat Pak Test Kit
(20 Tests)
FOR PROFESSIONAL USE ONLY! Clearview HIV 1/2 STAT-PAK Test Kit, is a rapid qualitative screening test for the detection of antibodies to HIV-1 and HIV-2 in human whole blood, serum and plasma. (FDA PMA#: BP050010) (NOT APPROVED FOR HOME USE-MEDICAL PROFESSIONALS ONLY)$269.99
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Quidel QuickVue Chlamydia Test
Quidel QuickVue Chlamydia Test
(25 Tests)
QuickVue Chlamydia Testing Kit, offers high sensitivity and specificity, in all patient populations. QuickVue is easy to perform and interpret. A simple extraction procedure requires the addition of only two reagents. FDA-Cleared and CLIA Classified Moderately Complex. (FDA 510K#: K946276)$309.95
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The QuickVue® Chlamydia offers high sensitivity and specificity — in all patient populations. The QuickVue® Chlamydia is easy to perform and interpret. A simple extraction procedure requires the addition of only two reagents. Either endocervical swab or cytology brush specimens can be used. The 25 test kit is stored at room temperature.BENEFITS:

  • Rapid Test Results: Provides timely results to aid patient management.
  • 92% Sensitivity (overall), 99% Specificity (overall) Accurate, reliable results for cost-effective patient care. 
  • 93.6% Sensitivity (asymptomatic), 99.1% Specificity (asymptomatic): Highly accurate in asymptomatic patient population. 
  • Two Reagents: Easy to perform — requires minimal training. 
  • Two-Color Endpoint: Easy to read and interpret results. 
  • Self-Contained Test Cassette: Clean, easy to use, easy to dispose. Less hands-on time. 
  • All Components Included in Kit: No need for additional equipment. 
  • Room Temperature Storage: No refrigerator space needed. No need for reagents to warm up. Tests can be run when needed. (9 months from date of manufacture) 

Quidel QuikVue Influenza Test

Quidel QuikVue Influenza Test
(25 Tests)
Detects Influenza type A and B viral (does not distinguish) antigens in three easy steps from a nasal swab or nasal aspirate/nasal wash specimen. Test results are available in 10 minutes or less. FDA Cleared and CLIA Waived. (FDA 510K#: K991633) NOT APPROVED FOR HOME USE! (IN-STOCK SHIPS same day up to 7pm EST) Expiration date approximately 1 year on this product!$339.95
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QuickVue Influenza Test:

The QuickVue Influenza test detects Influenza type A and B viral antigens in three easy steps from a nasal swab or nasal aspirate/nasal wash specimen. Test results are available in 10 minutes or less. The easy-to-use, easy-to-read kit can be stored at room temperature. No instrumentation is required. The 25-test kit offers bulk packaging that is ideal for batch testing. Kit includes everything to perform the test including positive and negative controls.

The QuickVue Influenza test is a simple, 3-step, 1-reagent, 10-minute test that requires less than 30 seconds hands-on time. The test has a shelf life of 24 months from date of manufacture and can be stored at room temperature. No additional instrumentation is required to perform the test. The QuickVue test is the first CLIA-waived rapid influenza test. With a specificity of 96-99%, the QuickVue Influenza test combines speed, simplicity and accuracy all in one test.

Feature: Benefit:
Two-color Result: Easy to read test results. Decreased risk of misinterpretation.
10 Minutes to Result: Allows prompt diagnosis and treatment while patient is still in office. Increases office efficiency and reduces patient follow up activities.
3 Step Procedure: Fewer procedural steps. Decreased risk of operator error.
Pictorial Procedure Guide: Simplifies understanding of testing procedure. Increases reliability.
Room Temperature Storage: No reagent warm-up. Use as needed without waiting. Does not take up refrigerator space.
12-18 Month Dating*: Economical test for low and high volume labs. Lasts up to 2 flu seasons.
Built-in Internal Control: Ensures system integrity.
Kit Includes External Controls: Facilitates internal laboratory quality control. No additional ordering needed.
Self Contained Kit Design: Components needed to run test are contained in sealed tray. Increases office efficiency.

The Clearview COMPLETE HIV 1-2 is a single-use, self contained, closed system for the collection, processing and analysis of a whole blood, serum or plasma sample for the detection of HIV 1 and HIV 2 antibodies in as little as 15 minutes.The Clearview COMPLETE HIV 1/2 will help healthcare workers diagnose individual infection, prevent mother-to-child transmission, and monitor HIV prevalence.BENEFITS:

  • Fast: two easy steps with a reactive result in as little as 15 minutes
  • Easy: Easy-to-use test; sample, process and analyze in a self contained system]
  • Reliable: built-in control ensures accuracy
  • Flexible: use with multiple specimen types – whole blood (fingerstick or venipuncture), serum, or plasma

OraSure Q.E.D. A-150 Saliva Alcohol Test
OraSure Q.E.D. A-150 Saliva Alcohol Test
(10 Tests) *NOW IN STOCK*
The OraSure Q.E.D. Saliva Alcohol test is a non invasive test. The test provides results in 2-5 minutes, reads like a thermometer,includes a built in quality control spot and offers a high correlation to blood alcohol. New stock! For in vitro diagnostic use. D.O.T. – Approved, FDA-Cleared and CLIA Waived. (FDA 510K#: K894001) All product has minimum 11-12 months shelf life$62.50
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The Q.E.D.® Saliva Alcohol test is a technological breakthrough that can be used as an accurate, quantitative measurement device for obtaining blood alcohol levels using a saliva sample. The test can reliably be used in place of blood, urine, or breath testing methods which require expensive equipment and operator training. Through a preset chemical reactive process that requires no user intervention, a color bar rises to the level of alcohol present in the system in much the same way as a mercury thermometer. In extensive clinical trials, saliva alcohol levels measured by the Q.E.D.® Saliva Alcohol test demonstrated a high correlation rate of 98% (r=0.98) to blood analyzed by sophisticated laboratory gas chromatography methods.BENEFITS:

  • Meets 2006 U.S. Coast Guard Maritime Requirements
  • Non Invasive, Quantitative Results in 2-4 Minutes
  • Interpretation like Reading a Thermometer
  • Long Shelf Life of 10-12 Months
  • Individually Sealed in Foil Envelope with Cotton Swabs
  • Built-in Quality Control and Calibration
  • U.S. DOT Approved for Testing and Evidence
  • High Correlation (r=.098) to Blood Analysis results
  • No Special Equipment or Training Required
  • FDA-Cleared/CLIA Waived



i-STAT Portable Clinical Analyzer Promo
i-STAT Portable Clinical Analyzer Promo
(1 Analyzer and Printer and Simulator)
CLIA-waived i-STAT Portable Clinical Analyzer – Blood Gas Test (Abbott Portable Handheld Clinical Analyzers). Promo instrument kit includes the Martel printer, a simulator, system manual and training manual. Serial downloader is sold separately! FDA-cleared and CLIA-waived.NOTE: All hardware comes with one-year manufacturer’s warranty. A optional service contract is available after the first year for $750 per annum. Service is on a swap-out basis.DISCLAIMER: The purchase of i-STAT analyzer and non-stocked i-STAT cartridges requires pre-approval and account set-up. Please call our office at 1-888-882-7739, Ext. 100 to set up an account.Request a QuoteMore Info
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Product Info: i-STAT 1
Lab-accurate without the wait.

This revolutionary, handheld analyzer provides reliable test results in just minutes, using as little as two drops of blood and a test cartridge.

The i-STAT® 1 handheld system performs a comprehensive panel of critical tests. Utilizing self-contained test cartridges, along with the Precision PCxand PCx Plus glucose test strips, the i-STAT 1 system delivers lab-accurate testing for Blood Gases, Electrolytes, Chemistries, Coagulation, Hematology, Glucose, and Cardiac Markers (cTnI).

It is portable, reliable, and includes these important features:

  • Easy To Use
    Cartridges are self-contained and the system is simple to  learn and operate

  • Lab-Accurate Results
    Advanced biosensor technology and real time quality assurance provides extremely accurate testing

  • Small Sample Size
    Just a few drops of blood per cartridge

  • Ready When You Need It
    Test results in as little as two minutes



BTA STAT – Rapid Test for Recurrent Bladder Cancer
BTA STAT – Rapid Test for Recurrent Bladder Cancer
(10 tests)
A Rapid Test For the Qualitative Detection of Bladder Tumor Associated Antigen in Human Urine. The BTA stat test is an in vitro immunoassay intended for the qualitative detection of bladder tumor
associated antigen in urine of persons diagnosed with bladder cancer. This test is indicated for use as an aid in the management of bladder cancer patients in conjunction with cystoscopy. FDA Cleared and CLIA waived. Use CPT HCPC CODE 86294 (QW) (National Limit is $27.61)$159.95More Info
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ABX Pentra 60 C+ Analyzer with Workstation
ABX Pentra 60 C+ Analyzer with Workstation
(1 System)
The ABX Pentra 60 C+ Analyzer is a small, convenient bench-top analyzer with excellent analytical performance for efficient patient care.Request a QuoteMore Info
Product Info

  • 60 CBC test/hour
  • 26 parameters
  • CLOSED tube (CT) sampling
  • Includes Data Management Workstation

New Instrument shipment includes:

  • Laser printer
  • UPS plus line conditioner
  • External barcode reader
  • Spare parts kit
  • Complete set of reagents
  • User Manual on CD
  • Interactive Product Training Video
  • Technical Phone Support
  • One year warranty on parts, labor and travel



Nano-Check AMI Cardiac Panel Test
Nano-Check AMI Cardiac Panel Test
(20 tests)
NEW! The Nano-Check AMI 3 in 1 cardiac panel is a lateral flow immunoassay for three key cardiac markers (TnI, CK-MB, Myo) in serum and heparin plasma samples. Nano-Check AMI aids in the early detection
of Acute Myocardial Infarction (AMI) in hospitals and physicans
offices. The results can be read visually for qualitative results. Compare to LifeSign at $499.95! (NOTE: This product is not CLIA Waived, Moderate Complexity.) FDA-Cleared (FDA 510K#: K050975)$250.00More Info
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Nano-Check™ 3 in 1 Test

  • Human Cardiac Troponin I/CK-MB and Myoglobin 3 panel test
  • Matrix: Whole Blood , Plasma , Serum
  • Detection Limit : 0.1 ng/ml for cTni, 2 ng/ml for CK-MB and 20 ng/ml of Myoglobin
  • Cutoff : 0.5 ng/ml for Tn I, 5 ng/ml for CK-MB and 80 ng/ml for Myoglobin
  • Sensitivity and Specificity : 98.1 and 99.1%

The Nano-Check TM AMI 3 IN 1 Test is a rapid immunoassay for the qualitative and quantitative determination of Cardiac Troponin I (cTnI), Creatine Kinase MB (CK-MB), and Myoglobin in human whole blood, serum and plasma specimens at cutoff concentrations of 0.5 ng/ml, 5.0 ng/ml, and 80 ng/ml respectively, as an aid in the diagnosis of Acute Myocardial Infarction (AMI). In conjunction with Nano-Checker 710 reader, the Nano-Check TM AMI 3 IN 1 Test can monitor the rise and fall of cTnI, CK-MB, and Myoglobin. Test results should be interpreted by the physician along with other test results and patient clinical symptoms findings.


  • Simple one-step test, contains all reagents necessary
  • Individually sealed pouch with dessicant
  • Can be used for whole blood, plasma, and serum samples
  • Easy-to-read results in 10-15 min.
  • Provides accurate quantitative controls.
  • For in vitro diagnostic use

Target:          Tnl/Myo/CK-MB
Specimen:    Whole Blood/Plasma/Serum
Format:         Cassette

Alere INRatio®2 PT/INR System

Alere INRatio®2 PT/INR System
(1 Monitor)
Formerly known as HemoSense, the Alere InRatio2 Monitoring System is a handheld coagulation system for monitoring patients taking wafarin. Used by healthcare professionals, the INRatio®2 provides accurate and convenient measurement of blood clotting time, or PT/INR values. Test strips are sold separately. FDA-cleared for professional use only. (FDA 510K#: K020679)$699.95
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The Alere INRatio®2 PT/INR Monitor connects reliable results with practical convenience, making it an optimal solution for anticoagulation management. It’s the #1 Best Seller at the Point of Care (HPIS comparative USA sales data, pointofcare PT/INR monitors sold 2005-2009).Benefits

  • On board quality control
  • Small sample size
  • Yields results in about 60 seconds
  • Allows the physician to make prompt medication changes
  • Facilitates discussion of dosage changes with patients
  • Improves patient satisfaction with simple fingerstick procedure
  • Maximizes practice efficiency by reducing time-consuming “call-backs”


  • Results print to the Alere INRatio® Printer*
  • Connects to a computer with PC Connect™ Software*
  • Easy to read display
  • Simple, icon-based interface
  • Built-in memory can store the INR results
  • AC or battery power
  • Battery supports up to 200 tests

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