Optimizing Your Sample Application Process

For the most optimized workflow when applying a patient or Quality Control sample to the Test Strip, please refer to the guidance provided in this Technical Bulletin, which is consistent with the instructions outlined in the Platform User Manual.

Applying a sample to the Test Strip

Following the insertion of a LumiraDx Test Strip, the Instrument display will prompt when to apply the sample. Apply ONLY one drop of the sample directly to the circular Sample Application Area on top of the Test Strip.

Page 1 Example:

The instrument display shows a timer counting down from 03:59, with a prompt to 'Apply sample to Test Strip' and 'Only apply one drop'.

Another screen shows a 'Sample Application' prompt, stating 'Only apply one drop. Sample detection may take up to 15 seconds.' The timer continues.

A 'Quality Control Test' screen shows 'Sample detected' and prompts to 'Close door to continue' with a timer of 00:14. Another screen shows 'Apply QC solution to Test Strip' with a timer of 01:55.

Visuals on page 1 depict applying a single drop of sample to the test strip with a red cross (❌) indicating an incorrect application and a green checkmark (✔️) indicating a correct application.

Important Notes on Sample Application

IMPORTANT: Sample detection and confirmation on the Instrument can take up to 15 seconds on some Test Strips. Whilst waiting for the confirmation, DO NOT apply any additional sample drops. If you think you have not applied the sample correctly, cancel the test on the Instrument, remove the Test Strip, and start another test using a fresh strip.

When the sample is detected, the Instrument will sound (if sounds are enabled) and a confirmation message will be displayed.

The touchscreen of the LumiraDx Instrument will request the user to close the door once the Instrument has detected the sample.

Removing the Test Strip from the LumiraDx Instrument

The Instrument will prompt to remove the Test Strip.

Gently pull the blue label end of the Test Strip to remove and dispose.

Do NOT bend the Test Strip when removing from the instrument. ⚠️

Page 2 Example:

The instrument display shows 'Test Complete' and prompts to 'Open door and remove Test Strip'.

Visuals on page 2 show the correct and incorrect methods of removing the test strip, with a red cross (❌) for incorrect removal and a green checkmark (✔️) for correct removal.

For further information refer to the “Preparation for Testing” chapter in the Platform User Manual for handling Test Strips, inserting and removing Test Strips and sample collection and application instructions.

Frequently Asked Questions

What do I do if I think I have applied too much sample to the Test Strip?

You can continue to use your Instrument. There are built-in checks to ensure the Instrument continues to operate accurately and safely. Take the Test Strip out carefully and do not bend the strip. If you have concerns, please contact Technical Services.

What do I do if I think I haven't applied enough Sample?

Sample detection and confirmation on the Instrument can take up to 15 seconds on some Test Strips. Whilst waiting for the confirmation, DO NOT apply any additional sample drops. If you think you have not applied the sample correctly, cancel the test on the Instrument, remove the Test Strip, and start another test using a fresh strip.

Product Enquiries and Technical Support

Please email or call Technical Services if you have questions.

Email: technicalservices.us@lumiradx.com

Phone: 1-888-586-4721

The LumiraDx SARS-CoV-2 Ag test has not been FDA cleared or approved but has been authorized by FDA under an EUA for use by authorized laboratories. This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens. The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug, and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated, or authorization is revoked sooner.

Copyright © 2023 LumiraDx UK LTD. All rights reserved worldwide. LumiraDx and Flame logo are trademarks of LumiraDx International LTD. Full details of these and other registrations of LumiraDx can be found at lumiradx.com/IP. All other trademarks are the property of their respective owners.

Content should be used for the use of the LumiraDx products only and in line with instructions provided. You may not, except with our express written permission, distribute or commercially exploit the content. Nor may you transmit it or store it in any other form of electronic retrieval system other than for the purpose of use of the LumiraDx Instrument, LumiraDx Instrument Base or LumiraDx Test Strips. Information provided is subject to change without notice.

Manufactured by: LumiraDx UK Ltd, Dumyat Business Park, Alloa, FK10 2PB, UK

Models: OS-04282-01, OS-04282-01 Test Strip, Test Strip, Strip

File Info : application/pdf, 3 Pages, 494.85KB

PDF preview unavailable. Download the PDF instead.

lumiradx-technical-bulletin-optimizing-your-sample-application-process-ivd-eua-r3

References

Adobe InDesign 19.0 (Macintosh) Adobe PDF Library 17.0

Related Documents

Preview LumiraDx Platform User Manual: Comprehensive Guide
This user manual provides detailed instructions for operating and maintaining the LumiraDx Platform, a point-of-care system for in vitro diagnostic tests. Learn about setup, testing procedures, troubleshooting, and safety information.
Preview LumiraDx Instrument Cleaning and Disinfection Procedure
This technical bulletin outlines the proper cleaning and disinfection procedures for the LumiraDx Instrument, including guidance for blood-based and swab-based samples, and recommended disinfectant materials.
Preview LumiraDx Platform Returns: A Comprehensive Guide
This document provides detailed instructions and guidance for returning the LumiraDx Platform, including procedures for data handling, disinfection, packaging, and shipping. It ensures proper return of instruments and associated materials for investigation and quality control purposes.
Preview LumiraDx SARS-CoV-2 Ag Test Fact Sheet for Healthcare Providers
This fact sheet provides information on the LumiraDx SARS-CoV-2 Ag Test, including its intended use, interpretation of results, and emergency use authorization by the FDA.
Preview LumiraDx SARS-CoV-2 Ag Test: Instructions for Use and Performance Data
This document provides comprehensive instructions for the LumiraDx SARS-CoV-2 Ag Test, including its intended use, assay principle, materials, warnings, precautions, sample collection and extraction procedures, test performance data, and interpretation of results. It is designed for healthcare professionals and authorized laboratories.
Preview LumiraDx SARS-CoV-2 Ag Test Specifications and Performance
Detailed specifications and clinical performance data for the LumiraDx SARS-CoV-2 Ag Test, an in vitro diagnostic test for the qualitative detection of SARS-CoV-2 nucleocapsid protein antigens.
Preview LumiraDx SARS-CoV-2 Ag Test: Quick Reference Instructions
Concise guide for performing the LumiraDx SARS-CoV-2 Ag Test, including sample preparation, running the test on the LumiraDx Platform, and interpreting results. For Emergency Use Authorization (EUA) only.
Preview LumiraDx SARS-CoV-2 Ag QC Transfer Pipettes Technical Bulletin
Technical bulletin detailing the use of QC transfer pipettes with the LumiraDx SARS-CoV-2 Ag Test, including acceptable pipette types and supplemental instructions for accurate sample dispensing.