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multi
plo®
Rapid
multiplo rapid tp hiv
Test

Accurate, rapid simultaneous detection of antibodies to HIV-1/2 and/or syphilis in whole blood, serum, and plasma specimens.

one test - two results

The Multiplo® Rapid TP/HIV Test enables simultaneous detection of antibodies to Treponema pallidum (syphilis) and HIV-1/2 in a single test using MedMira’s Rapid Vertical Flow (RVF) Technology™. Increasing co-infections – driven by shared risk factors and transmission routes – necessitate combined screening to support effective patient management and reduce mother-to-child transmission. Health Canada approved, our test provides fast, reliable point-of-care results from a single blood sample in just three simple steps. Its strong clinical performance supports timely decision-making, improving patient outcomes and contributing to broader public health goals.

  • Immediate results

    No waiting time, results do not vanish.

  • Reliable accuracy

    Achieves high testing performance.

  • Multiplex testing

    Multiple diseases tested on a single cartridge using one blood sample.

  • No equipment or refrigeration required

    Stores at room temperature (2–30 °C / 35–86 °F) with a 12-month shelf life.

  • Easy to use and interpret

    Simple procedure with instant, easy-to-read results, no special training required.

  • Ideal for POC setting

    Works with whole blood (fingerstick).

multiplo tp hiv
From sample to results

in three simple Steps

Testing doesn’t have to be complicated. Our intuitive three-step process ensures instant, consistent results with minimal effort.

Whole Blood
add buffer from v2 to blue cap
Pour buffer

Pour buffer onto the InstantGold™ cap.

TP HIV blood step2
Cap

Place the InstantGold™ cap on the cartridge.

TP HIV blood stept1
Add sample

Pour lysed blood specimen into the test cartridge.

For a detailed walkthrough, watch video (Youtube, 5:48 min)

Proven Results, Trusted Performance

The Multiplo® Rapid TP/HIV Test consistently delivers high overall clinical performance in rigorous evaluations and inspections.

100
HIV-1/2
Sensitivity (PPA; overall)
97.6
Specificity (NPA)
97.3
Sensitivity (PPA; ≥1:8)
99.2
Specificity (NPA)

Our test tailored to your needs

The Multiplo® Rapid TP/HIV Test is trusted in Canada for point-of-care use. Through regional distribution partners, we provide broad access to the POC format. It performs reliably in diverse and resource-limited settings without the need for specialized instruments, trained operators, or cold-chain storage. Our dual rapid test supports prenatal screening, public health STI programs, occupational exposure follow-up, counseling services, and mobile clinics – enabling earlier detection and reducing the risk of mother-to-child transmission.

Point-of-Care

This format includes a test tray in each pouch and is ideally suited to testing at the point of patient care, settings such as mobile clinics requiring a portable and all-in-one testing solution.

  • Cat. No. 815311004902
  • Qty. 20 tests per box
TP HIV POC

Downloads and Links

Additional materials are available through your partner login or upon request.

Product Specifications

Marketing Materials

Clinical Studies & Approvals

Further studies available upon request.

Related Products

Designed for use across POC settings, laboratories, academic institutions, and research environments.

Designed for use across POC settings, laboratories, academic institutions, and research environments.

Miriad is intended for laboratory, academic, and research use only, and is not for use in diagnostic procedures.

Learn more about our upcoming technology and products advancing through our development pipeline.

Frequently Asked Questions

To learn more about Multiplo® Rapid TP/HIV Test, please contact us.

How accurate is Multiplo® Rapid TP/HIV Test ?

The test demonstrates 83.8% overall sensitivity for Syphilis (TP) antibodies, with a specificity of 99.2%. For higher-titer Syphilis samples (≥1:8), sensitivity is 97.3%, and for lower-titer samples (<1:8), sensitivity is 88.1%. For HIV-1/2, the test provides 100% sensitivity and 99.6% specificity.

Where to buy Multiplo® Rapid TP/HIV Test?
You can purchase our products through authorized distributors in your region. Visit our ‘Partner’ page or contact our team for purchasing information in your region. For more information, contact sales@medmira.com.
Partners Contact Us
Why is dual HIV and syphilis testing essential?

HIV and syphilis are closely linked, as they spread through similar routes and often share the same risk factors. Syphilis can also increase the risk of HIV transmission, making co-infections more likely. With rising infection rates reported by ECDC and WHO, early dual screening has become increasingly important. A combined test delivers fast, efficient and accurate results and is especially valuable in pregnancy, helping prevent complications and mother-to-child transmission. Dual rapid tests are also simpler, more cost-effective, and more comfortable for patients, requiring only a single blood sample.

What makes Multiplo® Rapid TP/HIV Test different?

Multiplo® Rapid TP/HIV Test uses MedMira’s unique Rapid Vertical Flow (RVF) technology, which delivers instant results – significantly faster than conventional lateral flow assays. The RVF format requires only one buffer and features a single reaction window, reducing user steps and minimizing error potential. Unlike traditional tests that depend on strict timing or multiple wash steps, RVF provides timeless, easy-to-read results with no refrigeration or specialized equipment required. The technology offers laboratory-grade accuracy, low cost per test, and supports multiplexing for future assay expansion – combining speed, simplicity, and performance in a single platform.

What is RVF technology™?

RVF (Rapid Vertical Flow) is a flow-through technology that captures specific biomarkers from blood, serum, or plasma samples on a specialized membrane, delivering instant visual results.

Current Product Information for the U.S.

The Multiplo® Rapid TP/HIV Test is currently not authorized for diagnostic use under FDA regulations and is limited to non-diagnostic applications in the United States.

Explore your options with us

If you have any questions regarding the Multiplo® Rapid TP/HIV Test, its regulatory status in the U.S., or suitable research alternatives, please contact us for further information.

Current Product Information for the EU

The Multiplo® Rapid TP/HIV Test is currently not authorized for diagnostic use in the EU and is limited to non-diagnostic applications in CE-regulated markets.

Research Use Only Alternatives

For customers in the EU who require products for research applications, we recommend our Miriad® Research Use Only (RUO) product line. Please refer to the Miriad® RUO product pages for further details, and specifications.

miriad

Explore your options with us

If you have any questions regarding the Multiplo® Rapid TP/HIV Test, its regulatory status in the EU, or suitable research alternatives, please contact us for further information.

International

Outside North America, and the EU

one test - two results

The Multiplo® Rapid TP/HIV Test enables simultaneous detection of antibodies to Treponema pallidum (syphilis) and HIV-1/2 in a single test using MedMira’s Rapid Vertical Flow (RVF) Technology™. Increasing co-infections – driven by shared risk factors and transmission routes – necessitate combined screening to support effective patient management and reduce mother-to-child transmission. It provides instant results in a straightforward three-step process and is available in different formats suitable for laboratory and point-of-care use. Its proven performance supports reliable testing and timely clinical and public health decision-making.

  • Immediate results

    No waiting time, results do not vanish.

  • Reliable accuracy

    Achieves high testing performance across multiple specimen matrices.

  • Multiplex testing

    Multiple diseases tested on a single cartridge using one blood sample.

  • No equipment or refrigeration required

    Stores at room temperature (2–30 °C / 35–86 °F) with a 12-month shelf life.

  • Easy to use and interpret

    Simple procedure with instant, easy-to-read results, no special training required.

  • Ideal for any setting

    Works with serum, plasma, and whole blood (venipuncture or fingerstick).

multiplo tp hiv
From sample to results

in three simple Steps

Testing doesn’t have to be complicated. Our intuitive three-step process ensures instant, consistent results with minimal effort.

add buffer from v2 to blue cap
Pour buffer

Pour buffer onto the InstantGold™ cap.

TP HIV blood step2
Cap

Place the InstantGold™ cap on the cartridge.

TP HIV blood stept1
Add sample

Pour lysed blood specimen into the test cartridge.

For a detailed walkthrough, watch video (Youtube, 5:49 min)

add buffer to blue cap scale
Cap & Pour buffer

Place InstantGold™ cap on the test & 
add buffer.

TP HIV PlasmaSerum Step2
Add specimen

Apply specimen to the centre of the test membrane.

TP HIV PlasmaSerum Step1
Pour buffer

Apply buffer to the test center.

For a detailed walkthrough, watch video (Youtube, 2:11 min

Proven Results, Trusted Performance

The Multiplo® Rapid TP/HIV Test consistently delivers high overall clinical performance in rigorous evaluations and inspections.

100
HIV-1/2
Sensitivity (PPA; overall)
99.6
Specificity (NPA)
97.3
Syphilis
Sensitivity (PPA; ≥1:8)
99.2
Specificity (NPA)

Our test tailored to your needs

The Multiplo® Rapid TP/HIV Test is trusted worldwide for both point-of-care and laboratory settings. Working with regional distribution partners, we provide broad access to three formats designed for different testing environments.

Point-of-Care

This format includes a test tray in each pouch and is ideally suited to testing at the point of patient care, settings such as mobile clinics requiring a portable and all-in-one testing solution.

  • Qty. 20 tests per box
LAB+

The LAB+ format is designed for laboratory use, offering maximum flexibility for testing serum, plasma, and venipuncture whole blood with reliable and consistent results.

  • Qty. 50 tests per box
LAB S/P

The LAB S/P format is designed for laboratory use, ideally suited for serum and plasma specimens and batch testing, ensuring efficient processing and dependable performance.

  • Qty. 50 tests per box
TP HIV POC
TP HIV LAB plus
TP HIV LAB SP

Related Products

Designed for use across POC settings, laboratories, academic institutions, and research environments.

Designed for use across POC settings, laboratories, academic institutions, and research environments.

Miriad is intended for laboratory, academic, and research use only, and is not for use in diagnostic procedures.

Learn more about our upcoming technology and products advancing through our development pipeline.

Frequently Asked Questions

To learn more about Multiplo® Rapid TP/HIV Test, please contact us.

How accurate is Multiplo® Rapid TP/HIV Test ?

The test demonstrates 83.8% overall sensitivity for Syphilis (TP) antibodies, with a specificity of 99.2%. For higher-titer Syphilis samples (≥1:8), sensitivity is 97.3%, and for lower-titer samples (<1:8), sensitivity is 88.1%. For HIV-1/2, the test provides 100% sensitivity and 99.6% specificity.

Where to buy Multiplo® Rapid TP/HIV Test?
You can purchase our products through authorized distributors in your region. Visit our ‘Partner’ page or contact our team for purchasing information in your region. For more information, contact sales@medmira.com.
Partners Contact Us
Why is dual HIV and syphilis testing essential?

HIV and syphilis are closely linked, as they spread through similar routes and often share the same risk factors. Syphilis can also increase the risk of HIV transmission, making co-infections more likely. With rising infection rates reported by ECDC and WHO, early dual screening has become increasingly important. A combined test delivers fast, efficient and accurate results and is especially valuable in pregnancy, helping prevent complications and mother-to-child transmission. Dual rapid tests are also simpler, more cost-effective, and more comfortable for patients, requiring only a single blood sample.

What makes Multiplo® Rapid TP/HIV Test different?

Multiplo® Rapid TP/HIV Test uses MedMira’s unique Rapid Vertical Flow (RVF) technology, which delivers instant results – significantly faster than conventional lateral flow assays. The RVF format requires only one buffer and features a single reaction window, reducing user steps and minimizing error potential. Unlike traditional tests that depend on strict timing or multiple wash steps, RVF provides timeless, easy-to-read results with no refrigeration or specialized equipment required. The technology offers laboratory-grade accuracy, low cost per test, and supports multiplexing for future assay expansion – combining speed, simplicity, and performance in a single platform.

What is RVF technology™?

RVF (Rapid Vertical Flow) is a flow-through technology that captures specific biomarkers from blood, serum, or plasma samples on a specialized membrane, delivering instant visual results.

Privacy Policy

Last updated: April 20, 2026

MedMira Inc. (“MedMira”, “we”, “us”, or “our”) is committed to protecting personal information in accordance with applicable privacy laws, including the Personal Information Protection and Electronic Documents Act (PIPEDA) in Canada, as well as applicable United States and international privacy requirements.

This Privacy Policy describes how we collect, use, disclose, and safeguard personal information through our website. Our website is primarily informational in nature and does not provide user accounts, applications, or diagnostic services.

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Please Read These Terms Carefully Before Using This Site. This website is provided by MedMira Inc. (MedMira) and may be used for informational purposes only. By using the site or downloading materials from the site, you agree to abide by the terms and conditions set forth in this notice. If you do not agree to abide by these terms and conditions do not use the site or download materials from the site.

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Committed to quality
Certified & Proven Quality

Our quality management system is ISO 13485:2016 certified, compliant with the United States Food and Drug Administration’s current Good Manufacturing Practices (cGMP: Quality System Regulation Part 820 of CFR Title 21, Volume 8), European Union’s Directive 98/79/EC on in vitro diagnostic medical devices, and Health Canada Medical Device Regulations (SOR/98-282).

Additionally, we adhere to ISO 14971 (Application of Risk Management to Medical Devices) and ISO 2859 (Sampling Procedures for Inspection by Attributes). Certification and compliance to these requirements attests to our ability to maintain the highest standard of quality in medical device manufacturing, product development and corporate conduct.

Our products have been approved by regulators and UN agencies worldwide.

FDA

Health Canada

International Trade Centre (ITC)

Pan American Healtch Organization (PAHO)

UN Development Programme (UNDP)

UN Office for Project Services (UNOPS)

UN Office at Vienna (UNOV)

UN Population Fund (UNFPA)

United States Agency for International Development (USAID)

CFO & Head of Commercialization

Markus Meile

Markus joined MedMira in 2010, and moved into the role of Chief Financial Officer in 2014.

He previously served on the Company’s Board of Directors, as a member of the Audit Committee, and as the Senior Director of International Markets.

Prior to joining MedMira, Markus worked with a number of financial institutions in Switzerland, England, and Hong Kong. He holds a BSc from Royal Holloway University of London and has studied business management, strategic planning, investment and accounting at business school in Zurich. Previously, Markus worked in the medical device industry in Africa, Asia Pacific, and Europe.

He will combine his financial expertise with his broad range of international business knowledge to build financial and corporate strategies supporting MedMira’s continuing growth and increasing shareholder value.

Director of the Audit Committee, Nomination and Compensation Committee

Jianhe Mao

Jianhe Mao is the owner of Unipec, a consulting firm based in St. Gallen, Switzerland. Unipec focuses on helping European companies enter the Chinese market, through operational restructuring and ownership and management optimization.

In addition to leading Unipec, Mr. Mao is involved in several industrial projects and start-up ventures including Monsatec AG, a new company bridging the gap between laboratories and clinics with a cold plasma medical device. He serves on the boards of several European companies and is regarded as a trusted expert in legal cases, corporate corruption, operational turnarounds, and mergers and acquisitions.

Mr. Mao began his career as a project engineer and has gained experience in business development and real estate investment. He holds M.E. from Ruhr University Bochum.

CEO, Co-Founder & Co-Inventor

Hermes Chan, D.Sc. (h.c.)

Hermes Chan, our Chief Executive Officer and Co-Founder, leads our passionate and committed team in driving the strategic direction and growth of MedMira.

Hermes, who was named BioScience Innovator of the Year by The Economist in 2007, is the inventor of our patented rapid flow-through diagnostic technology platform.

Since the company’s inception in 1994 Hermes has held progressively senior management roles including Research Scientist, General Manager, Senior Vice President, and Chief Operating Officer.

Prior to creating MedMira, Hermes worked with another Canadian biotechnology company in the diagnostics research sector.

Chair member of the Audit Committee, Nomination and Compensation Committee

Steven Cummings

Mr. Steven Cummings is the Founder & President of Cambridge Financial Services, one of the leading full service accounting, tax, and business advisory firms in Nova Scotia.

Under Mr. Cummings leadership, Cambridge Financial has earned an enviable reputation among businesses and industry for a commitment to high standards. Along with his leadership responsibilities at Cambridge Financial Services, Mr. Cummings was engaged as MedMira’s interim Chief Financial Officer in 2007.

With more than 30 years of financial and entrepreneurial experience, Mr. Cummings is a frequent guest speaker on issues surrounding provincial taxation, taxation of seniors, and business ownership

Intellectual property

China

ZL02819646.5

Rapid Diagnostic Device and Assay

Intellectual property

European union

EP1417489

Rapid Diagnostic Device and Assay

EP1328811

HCV Mosaic Antigen Composition (2021)

Intellectual property

USA

9,164,087

Rapid Diagnostic Device, assay and multifunctional Buffer

9,086,410

Downward or vertical flow diagnostic device and assay

8,025,850

Rapid Diagnostic Device, Assay and Multifunctional Buffer

8,287,817

Rapid Diagnostic Device, Assay and Multifunctional Buffer

8,586,375

Rapid Diagnostic Device, Assay and Multifunctional Buffer

7,531,362

Rapid Diagnostic Device, Assay and Multifunctional Buffer

D706945

Diagnostic Device

D706466

Diagnostic Device

11,353,450

Analyte Detection Using Raman Spectroscopy

Intellectual property

Canada

CA2,493,616

Rapid Diagnostic Device, Assay and Multifunctional Buffer

CA2,740,902

Downward or Vertical Flow Diagnostic Device and Assay

CA2,949,634

Analyte Detection Using Raman Spectroscopy

MiROQ Vision

Handheld Device

A future concept built on the same MIROQ technology, designed to deliver lab-grade precision in the palm of your hand.

We envision a future where testing can happen anywhere, anytime – from hospitals and clinics to remote regions or even at home – enabling early disease detection and turning knowledge into real impact. No large equipment or complex infrastructure required.

For: Doctor’s offices, small and mobile clinics

Future application: Home use

Connectivity: Bluetooth, Wifi and USB