Be Sure - LC-MS Medical Devices for Laboratory Developed Tests

With so much riding on something so small, why would you choose anything else? Be sure.

Every sample analyzed in your clinical laboratory carries the weight of doctors and patients waiting for the direction your results provide. Leveraging the very best analytical instruments allows you to BE SURE of the quality of your results and timeliness of your reports. The new portfolio of LC-MS Medical Devices provides laboratories with comprehensive and reliable LC-MS systems powered by a complete suite of software conforming to in vitro diagnostic (IVD) requirements and offering an optional laboratory information system (LIS) connection enabling clinical diagnostic laboratories to reach their business and scientific goals for laboratory developed tests (LDTs).

Increase efficiency, throughput, and cost savings— performing laboratory developed tests by liquid chromatography-mass spectrometry
Vanquish MD HPLC
TSQ Quantis MD Series Mass Spectrometer
TSQ Altis MD Series Mass Spectrometer
Prelude MD HPLC
Prelude LX-4 MD HPLC
Vial of Blood in Hand

Liquid Chromatography Mass Spectrometry for Laboratory-Developed Tests

Find the solution best suited for your laboratory's needs in terms of sensitivity, selectivity, and throughput. Contact our solutions specialists to learn more.

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For in-vitro diagnostic use. Specifications subject to change. Availability of product in each country depends on local regulatory marketing authorization status.

This information is presented as an example of the capabilities of Thermo Fisher Scientific products. It is not intended to encourage use of these products in any manner that might infringe the intellectual property rights of others. Specifications, terms and pricing are subject to change. Thermo Fisher Scientific is in the process of ensuring that the Vanquish MD HPLC system, Prelude LX-4 MD HPLC system, TSQ Altis MD mass spectrometer, and TSQ Quantis MD mass spectrometer comply with all regulatory requirements for application of the CE mark under the new IVDR requirements.