The fNIR Imaging Systems from fNIR Devices offer a stand-alone, non-invasive solution for continuous functional near-infrared spectroscopy (fNIRS), enabling real-time monitoring of brain activity without the constraints of traditional imaging modalities like fMRI. Subjects can remain seated at a computer or engage in mobile tasks, making it ideal for naturalistic cognitive function assessments.
fNIRS is an optical neuroimaging method that measures brain activity by detecting changes in blood oxygenation in the prefrontal cortex. The sensor band, which contains infrared light sources and detectors, is worn comfortably on the forehead. As the subject performs tasks, the system continuously captures real-time changes in oxy- and deoxy-hemoglobin levels, providing valuable insights into cognitive processes.
The Imager 2000S supports up to 54 channels for high-resolution, continuous NIR spectroscopy and includes:
fNIRS data can be seamlessly synchronized with other physiological measurements, such as:
When combined using AcqKnowledge software, researchers can perform advanced analyses like event-related potentials (ERPs) and ensemble averaging, enabling deeper insights into the subject’s physiological and cognitive states. Applications include:
fNIRS integrates smoothly with BIOPAC’s virtual reality platforms and stimulus delivery tools.
fNIRSoft (fS) Pro is a standalone software suite for acquisition, visualization, and advanced analysis of fNIRS data. Users can interact via a graphical user interface or automate tasks through scripting. Key features include:
fS Pro enhances the research workflow with extended functionality compared to the standard version, enabling advanced exploration of brain activation patterns.
For experiments involving multiple physiological signals, fNIR Systems can be synchronized with BIOPAC’s MP200 Research System:
This integration enables precise alignment of fNIRS data with other biosignals for high-quality, time-locked analyses.
Important Note: This product is for research applications only. Not a medical device as defined in Regulation (EU) 2017/745 (EU MDR), Swiss Medical Devices Ordinance (MedDO, SR 812.213), or FDA 21 CFR Part 860. Not designed or intended to be used for diagnosis, treatment of disease or any other medical purposes.