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Rapid COVID-19 LAMP International Travel Test With Results In 30 Minutes

Rapid COVID-19 LAMP International Travel Test With Results In 30 Minutes

Speed Of A Rapid Antigen Test

Accuracy Of A PCR

Need a Rapid COVID-19 LAMP International Travel Test with results in 30 minutes and the a report in just a few hours?

We can do it with our LAMP Test! Click below to learn more and purchase.

We charge $175 for this hyper fast, high speed turnaround rapid COVID-19 test.

While we target reports in 3 hours, sometimes they can take longer. This is a relatively new test. We do not offer refunds for inconclusive results.

THIS IS NOT A PCR TEST! SOME COUNTRIES ACCEPT THE L.A.M.P. TEST, BUT MANY DO NOT!

Rapid COVID-19 LAMP International Travel Test With Results In 30 Minutes.

uMedMarket offers custom L.A.M.P. Testing most mornings between ~6:30-7:30am on weekdays and 7:30-8:30am on weekends in Greenville, SC with results in a few hours (generally), usually by noon (if you need a custom collection time, we can totally do it, please just contact us). This is how it works:

  1. Read ALL the instructions below.
  2. Fill out the form linked below. It will ask things like what day you’d like to get tested, demographic information (gender, DOB, name, home address, etc), and payment information. We do not recommend you schedule mission critical tests within 12 hours of your deadline. Schedule for as early as you can in your window of availability. All the fields are required by state law.
  3. You will pay $175 via credit card as part of filling out the form. Cancellations for any reason will incur a $30 fee.
  4. Once you’ve paid, we will send you a Calendar Invite for the collection appointment with all the information you need like time and location. This may take a few hours because this is a manual process.
  5. You come to the location in the calendar invite (about 1 mile from downtown Greenville, in an old bank parking lot) and pull up by the cones. You do not need to get out of your car and DO NOT GO IN THE BUILDING. Testing will occur at 901 Grove Rd, Greenville, SC 29605.
  6. I will come to you with the collection kits and supervise a mid-turbinate nasal self-collection. I will be wearing a mask and gloves and keep a 6 foot distance between us at all times.
  7. You will receive an email with a link to a PDF of your lab report (click here to see a sample report) typically within a few hours of testing. Add us (contact@uMedMarket.com) to your email whitelist so our email does not get blocked by your spam filter. You can download, print, save or email the report as you wish. While we target  reports to be sent in 3 hours or less, sometimes it takes a bit longer. We are not responsible for inconclusive results and cannot give a refund if inconclusive. This test looks for 2 markers and if one is positive and the other negative, you have too many markers to be negative, but not enough to be positive.
  8. Collection times are listed on the report.

Click Here To Purchase The L.A.M.P. Test For $200

What's The Difference Between LAMP And PCR?

Rapid L.A.M.P. Test

Loop-mediated isothermal amplification
$ 175
  • Molecular
  • FDA Emergency Use Authorized (EUA)
  • Highly Accurate
  • Report Has CLIA Number
  • Results In 30min, Report In A Couple Hours
  • Only Accepted By A Few Major Countries (And Most Of EU)
  • Any Age Accepted
  • Nasal Swab Only
Faster

PCR

Polymerase chain reaction
$ 200
  • Molecular
  • FDA Emergency Use Authorized (EUA)
  • Highly Accurate
  • Report Has CLIA Number
  • Results Generally In 12-18 Hours
  • Generally Accepted For Worldwide Travel
  • Any Age Accepted
  • Nasal Swab Or Saliva
Widely Accepted

LAMP Test: Speed Of An Antigen Test, Accuracy Of A PCR Test

Rapid COVID-19 LAMP International Travel Test With Results In 30 Minutes

LAMP Test Data And Details:

This test, the Lucira COVID-19 All-In-One Test Kit, has not been FDA cleared or approved, but is authorized by the FDA under it’s Emergency Use Authorization (EUA) and can be found listed here: https://www.fda.gov/emergency-preparedness-and-response/mcm-legal-regulatory-and-policy-framework/emergency-use-authorization.

Lucira’s COVID-19 All-In-One Test Kit is a molecular in vitro diagnostic test that has an analytical sensitivity, or ability to detect the SARS-CoV-2 virus, that is comparable to some of the best molecular tests performed in clinical settings and high complexity labs. In a Community Testing Study, where the Lucira test was compared to a FDA authorized known high sensitivity SARS-CoV-2 test, Lucira achieved a 94% positive percent agreement (PPA) and a 98% negative percent agreement (NPA). Excluding samples with very low levels of virus that possibly no longer reflected active infection (La Scola B., Clinical Infectious Diseases, September 2020), Lucira achieved 100% positive percent agreement.

The information in this report is designed and intended to be interpreted by a licensed medical professional or physician. It is not meant to take the place of or provide medical advice or guidance.Medical actions and treatment should be sought from a licensed healthcare professional who can account for medical context and history. Negative results do not preclude SARS-CoV-2 infection. Individuals who

test negative and continue to experience COVID-like symptoms should seek follow up care from their healthcare provider.
Codes and Identifiers

Test Type: RT Loop-mediated isothermal amplification (RT-LAMP)
Test Ordered (LOINC Code):  95409-9
Device Identifier:  00810055970001



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