-

QIAGEN Launches QIAcube Connect MDx Platform for Automated Sample Processing in Diagnostic Labs

  • QIAcube Connect MDx carries CE-IVD marking in Europe and will be launched globally
  • Device allows labs to use in-vitro diagnostics (IVD) and more than 140 other QIAGEN standard protocols
  • Platform builds on success of over 9,800 installed QIAcube and QIAcube Connect instruments

GERMANTOWN, Md. & HILDEN, Germany--(BUSINESS WIRE)--QIAGEN N.V. (NYSE: QGEN; Frankfurt Prime Standard: QIA) today announced the global launch of the QIAcube Connect MDx, a flexible platform for automated sample processing that will now be available to molecular diagnostic laboratories in the U.S. and Canada, the European Union and other markets worldwide.

QIAcube Connect MDx is an enhanced instrument from the QIAcube product line for in-vitro diagnostic applications (IVD) that tests samples taken from the human body. The fully automated, flexible system with diagnostic and research protocols can be used in combination with QIAGEN’s gold standard QIAamp DSP kits and PAXgene Blood RNA extraction kits.

This expansion to clinical applications complements the use of QIAcube Connect and the QIAcube HT instruments in life science applications. QIAGEN has placed more than 9,800 instruments of the QIAcube instrument family by the end of 2020. It also further enhances QIAGEN’s automated sample preparation portfolio led by the QIAsymphony flagship system.

The new QIAcube Connect MDx version is compliant with medical device design standards and regulations and increases lab-process safety with a complete IVD system, which can also be used to prepare SARS-CoV-2 and other viral samples for diagnostic testing. The platform can be used with over 80 QIAGEN kits and more than 140 standard protocols and ensures full standardization of the purification of multiple sample types.

Researchers can be freed up from repetitive and costly manual processing by allowing laboratories to automate the first steps of molecular diagnostic workflows through the use of QIAGEN’s gold-standard spin column technologies for DNA, RNA and protein sample processing.

Please find the full press release here.

For more information about QIAcube Connect MDx platform, please visit our product page. Further information on QIAGEN’s response to the coronavirus outbreak can be found here.

Contacts

QIAGEN
Investor Relations
John Gilardi, +49 2103 29 11711
Phoebe Loh, +49 2103 29 11457
e-mail: ir@QIAGEN.com

Public Relations
Thomas Theuringer, +49 2103 29 11826
Robert Reitze, +49 2103 29 11676
e-mail: pr@QIAGEN.com

QIAGEN N.V.

FWB:QIA
Details
Headquarters: Venlo, Netherlands
CEO: Thierry Bernard
Employees: 5800
Organization: PUB
Revenues: US$ 1.97 billion (2023)
Net Income: US$ 341.3 million (2023)

Release Summary
QIAGEN launches QIAcube Connect MDx platform for automated sample processing in diagnostic labs
Release Versions
$Cashtags

Contacts

QIAGEN
Investor Relations
John Gilardi, +49 2103 29 11711
Phoebe Loh, +49 2103 29 11457
e-mail: ir@QIAGEN.com

Public Relations
Thomas Theuringer, +49 2103 29 11826
Robert Reitze, +49 2103 29 11676
e-mail: pr@QIAGEN.com

Social Media Profiles
More News From QIAGEN N.V.

QIAGEN to Showcase New Sample to Insight Solutions for Complex Oncology Applications at AACR 2026

GERMANTOWN, Md. & VENLO, Netherlands--(BUSINESS WIRE)--QIAGEN N.V. (NYSE: QGEN; Frankfurt Prime Standard: QIA) today announced it will showcase its oncology workflow applications at the American Association for Cancer Research (AACR) Annual Meeting 2026 in San Diego, demonstrating how its portfolio connects sample preparation with multi-omics profiling and genomic data interpretation to support cancer research and molecular diagnostics. “Cancer research and molecular diagnostics are increasingl...

QIAGEN Expands Into Bloodstream Infection Syndromic Testing With New Rapid QIAstat-Dx Panel

HILDEN, Germany & VENLO, Netherlands--(BUSINESS WIRE)--QIAGEN N.V. (NYSE: QGEN; Frankfurt Prime Standard: QIA) today announced its expansion into syndromic testing for bloodstream infections with the launch of the CE-IVDR-certified QIAstat-Dx BCID GPF Plus AMR Panel. The launch of this new QIAstat-Dx panel coincides with the ESCMID Global 2026 Congress in Munich (April 17–21), where QIAGEN will highlight its broad infectious disease portfolio, including QIAstat-Dx, the QuantiFERON-TB Gold Plus...

Qiagen Announces Form 20-F Annual Report Filing for 2025 Results

VENLO, the Netherlands--(BUSINESS WIRE)--QIAGEN N.V. (NYSE: QGEN; Frankfurt Prime Standard: QIA) announced today that it has filed its annual report, including its audited consolidated financial statements on Form 20-F, for the year ended December 31, 2025, with the U.S. Securities and Exchange Commission. The document can be accessed on QIAGEN’s website here. QIAGEN will provide printed copies of the 2025 Annual Report to shareholders free of charge upon request. To obtain a printed copy of th...
Back to Newsroom