LifeSign Made in USA

LifeSign Made in USA

Strep A-FLIP

Rapid Detection Of Group A Streptococcal Antigen Directly From Throat Swab Specimens

  • CLIA WAIVED
  • Single use reagent capsules
  • Positive results in 5 min
  • Sensitivity 96%, specificity 99%
  • No counting reagent drops – fewer steps for greater accuracy
Product Insert

Flu/COVID-19 Ag A Rapid Immunoassay for the Simultaneous Direct Detection and Differential Diagnosis of SARS-CoV-2, Influenza Type A and Type B Antigen from nasal or nasopharyngeal swab specimens

  • FDA Emergency Use Authorization (EUA)
  • Visually read in 15 minutes
  • Flocked swab for superior specimen collection and patient comfort
  • 25 tests per box
Product Insert

Status™ Flu A&B, CLIA Waived, for nasal and NP swab specimens

  • CLIA WAIVED for nasal swab and nasopharyngeal swab specimens
  • Rapid diagnosis for early treatment
  • 25 tests per box
  • Innovative flip test design
  • Easy-to-read cassette
  • Pre-measured extraction reagent capsule for increased accuracy and ease of use
  • Flocked nasal swabs included for better specimen collection
  • Detects H1N1 (Swine Flu)
Product Insert

LifeSign MI Troponin I

  • Qualitative Troponin I
  • Enables prompt emergency room decisions
  • Easy to use procedure; Add 3 drops of specimen into device
  • Read results in 15 minutes
  • Improves patient care
  • Reduces unnecessary testing and admissions
Product Insert

LifeSign MI CK-MB/Myo/TnI

  • MODERATELY COMPLEX
  • Qualitative CK-MB, Myoglobin, Troponin I
  • Enables prompt emergency room decisions
  • Easy to use procedure; Add 3 drops of specimen into device
  • Read results in 15 minutes
  • Multiple panel assays
  • Improves patient care
  • Reduces unnecessary testing and admissions


Product Insert

COVID-19/Flu

  • MODERATELY COMPLEX
  • Qualitative CK-MB, Myoglobin, Troponin I
  • Enables prompt emergency room decisions
  • Easy to use procedure; Add 3 drops of specimen into device
  • Read results in 15 minutes
  • Multiple panel assays
  • Improves patient care
  • Reduces unnecessary testing and admissions


Product Insert

Status hCG serum/urine


  • Designed to detect hCG in serum or urine
  • CLIA waived for urine
  • Serum and urine 25 mIU/mL sensitivity
  • Physician’s licensing required. This is NOT an at-home test and should only be completed in a lab facility


Product Insert

Status iFOBT

  • CLIA Waived
  • Superior sensitivity and specificity
  • Human hemoglobin specific for reducing false positives
  • Easy one-step test procedure
  • Specimen can be collected in office or at home
  • Patient friendly and easy-to-follow instructions
  • Non-invasive collection method
  • Only one test device needed
  • No dietary or drug restrictions for iFOBT
Product Insert

Status™ COVID-19 Antigen Rapid Test For Home Use (1)

  • 1 Test per box
  • FDA Emergency Use Authorization (EUA)
  • Visually Read in 15 minutes
  • For Home Use, Workplace Testing, Schools
Product Insert

Status™ COVID-19 Antigen Rapid Test For Home Use (25)

  • 25 Tests per box
  • FDA Emergency Use Authorization (EUA)
  • Visually Read in 15 minutes
Product Insert

Status DS

  • 25 Tests per box
  • Simple one-step procedure
  • Accurate results with a 97-99% correlation to GC/MS
  • Fast turnaround time with results in 5-10 minutes
Product Insert

Status MONO

  • CLIA WAIVED for whole blood
  • FDA cleared with no age restrictions
  • Single reagent procedure provides results in 3-8 minutes
  • Fingerstick whole blood convenience
  • Superior 99.9% sensitivity for earlier IM detection, specificity of 98.8%
  • Multiple kit sizes available, ideal for any practice
  • External QC negative and positive controls included (item # 68364 & 84M30)
  • New plastic sample transfer pipettes
Product Insert

Status Nicotine

  • Simple one-step procedure
  • Results in as little as 5-10 minutes
  • 500 ng/mL cut-off detects active nicotine intake
  • Useful in immediate counseling and intervention
Product Insert

Uricult (Urinary Tract Infections)

  • Moderately Complex
  • Culture method for urinary pathogens
  • Easy to perform procedure; Dip - Incubate - Read Results
  • Quick and convenient result within 24 hours
  • Simple CLIA compliance for reporting colony counts.
CLED EMB Product Insert CLED+Pol MC Product Insert CLED Poly EMB Product Insert

Alco-Screen is a rapid, highly sensitive method to detect the presence of alcohol in saliva and provide an approximation of relative blood alcohol concentration. Since it is well established that the concentration of alcohol in saliva is very close to that in the blood, saliva is the preferred specimen for alcohol testing, allowing for greater detection sensitivity than breath testing methods. Alco-Screen is a very simple, one-step, 2 minute test requiring no instrumentation, calibration or special training to be used effectively, and is convenient enough to be used any time, any place.

Alco-Screen Saliva Alcohol Test

Testing with the Alco-Screen saliva alcohol test is fast and easy.  The operator has the subject spit into a cup and dips the reagant tip of the strip into the saliva for several seconds. The Alco-Screen requires such a small amount of saliva to activate the test, even subjects with dry mouth can be tested successfully. Results are visible within two minutes after wetting the test strip with saliva.


Alco-Screen Estimates Alcohol Concentration

Because the proportion of alcohol in saliva is directly related to the proportion of alcohol in blood, the Alco-Screen can easily and quickly detect the presence of alcohol and estimate intoxication levels. The presence of alcohol in saliva causes the reagent pad to turn shades of green. Higher concentrations of alcohol create darker shades of green. The operator estimates intoxication levels by comparing the color change against color standards printed on the foil package at the 0.02%, 0.04%, 0.08%, and 0.30% BAC.


Ideal for Zero Tolerance Testing

The Alco-Screen is ideal for agencies with zero tolerance policies and for non-regulated employee workplace testing programs. Any green color on the reagent pad after two minutes indicates the presence of alcohol in the saliva of at least 0.02% or greater. 0.02% BAC is approximately the intoxication level from one drink, and is typically the lowest cut-off level used to determine if a person has been drinking alcohol.


Alco-Screen Detects Alcohol in Beverages

The Alco-Screen is one of the few devices that can detect the presence of alcohol in beverages. Because the Alco-Screen is calibrated to detect the very tiny amounts of alcohol present in saliva, the color standards on the test do not apply when testing beverages. The concentration of alcohol is extremely high in comparison to saliva. Dipping the strip into a beverage that contains alcohol causes the reagent pad to turn a very dark brown color.

STEP 1 – Collect a subject’s saliva in a clean, unused cup and dip the reagent end of test strip in the cup for several seconds. Once the reagant pad is saturated with the saliva, place the strip on a flat surface and set a 2 minute timer.


STEP 2 – After 2 minutes compare the color change against the color standards on the back of the envelope package to estimate alcohol level.

On-Site Testing Specialists provides this exam and certification to evaluate the knowledge of an individual in regards to specimen collection, device testing  and test interpretation according to the manufacturers recommendations. This certification is NOT an accredited certification for DOT or workplace specimen collection/testing. 

Take Exam

Quick 4 Minute On-Site Test for Alcohol

  • Convenient use anywhere anytime
  • FDA Cleared
  • DOT Approved
  • CLIA Waived 
  • Over the counter use
  • 24 tests per box
Product Insert

Alco-Screen® 02 is a simple, cost effective tool used to monitor alcohol consumption as part of a comprehensive Zero Tolerance testing program. Alco-Screen® 02 is a Conforming Product for US Department of Transportation mandated testing of all transportation and safety sensitive employees for blood alcohol concentrations above the federally mandated zero tolerance level of 0.02%. Alco-Screen® 02 is FDA 510(k) cleared for home use and is CLIA waived.


Convenient, Fast Results

Testing with the Alco-Screen® 02 is as easy as placing one end of the test strip in the subjects mouth for a few seconds to wet it with saliva. The operator reads results in four minutes.

Estimates Alcohol Concentration

Because the proportion of alcohol in saliva is directly related to the proportion of alcohol in blood, the Alco-Screen® 02 can easily and quickly detect the presence of alcohol and estimate intoxication levels. The presence of alcohol in saliva causes the reagent pad to turn shades of green. Higher concentrations of alcohol create darker shades of green. The operator estimates intoxication levels by comparing the color change against color standards printed on the foil package at the 0.02%, 0.04%, 0.08%, and 0.30% BAC.


Ideal for Zero Tolerance Testing

The Alco-Screen® 02 is ideal for agencies with zero tolerance policies. Any green color on the reagent pad after two minutes indicates the presence of alcohol of at least 0.02% or greater. 0.02% BAC is about the intoxication from one drink and is typically the lowest cut-off level used to determine if a person has been drinking alcohol.


Detects Alcohol in Beverages

The Alco-Screen® 02 is one of the few devices that can detect the presence of alcohol in beverages. Because the Alco-Screen is calibrated to detect the very tiny amounts of alcohol present in saliva, the color standards on the test do not apply when testing beverages. The concentration of alcohol is extremely high in comparison to saliva. Dipping the strip into a beverage that contains alcohol causes the reagent pad to turn a very dark brown color.



Alco-Screen® 02 is a one-step saliva screening test that is minimally invasive and provides results within 4 minutes. Simply wet the test pad with saliva; development of a distinct colored line on the test pad within 4 minutes indicates a blood alcohol concentration equal to or exceeding 0.02%


DOT Approved as Alcohol Screening Device

The Alco-Screen® 02 was one of the first devices to be approved by the U.S. Department of Transportation (DOT) as an Alcohol Screening Device. DOT approval means that the Alco-Screen reliably and accurately detects alcohol at the 0.02 concentration or higher and does not give false positive readings when no alcohol is present. DOT approval allows users to use the Alco-Screen® 02 for screening tests required by Dept. of Transportation regulations.

On-Site Testing Specialists provides this exam and certification to evaluate the knowledge of an individual in regards to specimen collection, device testing  and test interpretation according to the manufacturers recommendations. This certification is NOT an accredited certification for DOT or workplace specimen collection/testing. 

Take Exam

ETG Alcohol Urine Tests

  • 25 Urine alcohol test kits for Ethyl Glucuronide (EtG)
  • Up to 80 hour detection time!
  • 12-18 month expiration date on all urine drug test cards (guaranteed)
  • Fast results in 5 minutes


Product Insert

The One Step Drug of Abuse Test is a competitive immunoassay utilizing highly specific reactions

between antibodies and antigens for the detection of multiple drugs and drug metabolites in

human urine.

The One Step Drug of Abuse Test is a rapid urine screening test that utilizes monoclonal

antibodies to selectively detect elevated levels of specific drugs in urine without the use of an

instrument.

The One Step Drug of Abuse Test is an immunoassay based on the principle of competitive

binding. Drugs which may be present in the urine specimen compete against their respective drug

conjugate for binding sites on their specific antibody.

During testing, a urine specimen migrates upward by capillary action. A drug, if present in the urine

specimen below its cut-off concentration, will not saturate the binding sites of its specific antibody.

The antibody will then react with the drug-protein conjugate and a visible colored line will show up

in the test line region of the specific drug strip. The presence of drug above the cut-off

concentration will saturate all the binding sites of the antibody. Therefore, the colored line will not

form in the test line region.

A drug-positive urine specimen will not generate a colored line in the specific test line region of the

strip because of drug competition, while a drug-negative urine specimen will generate a line in the

test line region because of the absence of drug competition.

To serve as a procedural control, a colored line will always appear at the control line region,

indicating that proper volume of specimen has been added and membrane wicking has occurred.

Allow the test device and urine speimen to come to room temperature [15-30oC (59-86oF)] prior to

testing.

[For Strip]

1) Remove the strip from the foil wrapper or the desiccated container (bring the container to the room

temperature before opening to avoid condensation of moisture in container). Label the strip with patient

or control identifications.

2) Immerse the strip into the urine with the arrow end pointing toward the urine. Do not cover the urine

over the MAX (maximum) line. You may leave the strip in the urine or you may take the strip out after a

minimum of 15 seconds in the urine and lay the strip flatly on a non-absorptive clean surface.

3) Read results at 5 minutes.

 DO NOT INTERPRET RESULT AFTER 10 MINUTES.

[For Cassette]

1) Remove the test device from its foil wrapper by tearing along the slice (bring the container to the room

temperature before opening to avoid condensation of moisture in container). Label the device with

patient or control identifications.

2) Using the specimen dropper, withdraw the urine sample from the specimen cup and slowly dispense 3

drops (approximately 120uL) into the circular sample well, being careful not to overfill the absorbent

pad.

3) Read results at 5 minutes. DO NOT INTERPRET RESULT AFTER 10 MINUTES.


[For Dipcard]

1) Remove the test device from the foil pouch.

2) Remove the cap from the test device. Label the device with patient or control identifications.

3) Immerse the absorbent tip into the urine sample for 5 seconds. Urine sample should not touch the

plastic device.

4) Replace the cap over the absorbent tip and lay the device flatly on a non-absorptive clean surface.

5) Read results at 5 minutes.DO NOT INTERPRET RESULT AFTER 10 MINUTES.

[For Multi-Drug Screen Test Cup]

Please follow the instructions on the Procedure CardAlco-Screen® 02 is a one-step saliva screening test that is minimally invasive and provides results within 4 minutes. Simply wet the test pad with saliva; development of a distinct colored line on the test pad within 4 minutes indicates a blood alcohol concentration equal to or exceeding 0.02%


DOT Approved as Alcohol Screening Device

The Alco-Screen® 02 was one of the first devices to be approved by the U.S. Department of Transportation (DOT) as an Alcohol Screening Device. DOT approval means that the Alco-Screen reliably and accurately detects alcohol at the 0.02 concentration or higher and does not give false positive readings when no alcohol is present. DOT approval allows users to use the Alco-Screen® 02 for screening tests required by Dept. of Transportation regulations.

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