Maximum Channels:
8: SPO2, PPG, pulse rate, activity (movement), heart sounds, respiration inhalation and exhalation patterns, airflow, snoring
Scientifically-validated and
editable autoscored full disclosure signals with forehead-based self-application. For multinight evaluation of sleep
architecture and sleep continuity in home or hospital,
with auto-detection of sleep
biomarkers associated with
neurodegeneration. PSG2 upgrade enables auto-detection of apneas, hypopneas and RERAs, and REM-related SDB severity. 5: Plethysmogram, pulse rate, heart rate variability, oximetry, actigraphy 8: airflow, snore, SpO2, pulse rate, chest effort,
body position, CPAP pressure, PPG 13: thoracic/abdominal effort, pressure, pressure-based
snore, snore sensor, thermistor, SpO2, pulse rate, plethysmography, body position, 3
channels ExG 16: 2x frontal EEG, 2x EOG chin, EMG, nasal cannula, chest and abdomen effort (RIP belt), SpO2, 2-lead ECG (heart rate), pulse 2x, leg EMG, audio, body position 8: heart rate, pulse
oximetry, respiratory airflow (CPAP compatible), RIP belt, snore, body
position, auxiliary (second RIP, thermal airflow, or IDcheck), actigraphy 13: nasal pressure, snoring, CPAP mask pressure, thoracic and abdominal effort, body position, SpO2, pulse rate, plethysmography waveform, signal quality, limb movement (or optional nasal thermistor), 2xEXG (EEG, EOG, EMG, ECG, or off) 9: EEG sleep staging, airflow (cannula or Bi/CPAP interface), Bi/CPAP pressure, respiratory effort (RIP), snore, SpO2, pulse rate, plethysmography, tri-axis body position 13: 2x RIP, pressure
transducer, SpO2, pulse, plethysmography, body position, 2x ExG; 3x DC channels, luminosity sensor 19: pressure, sound, gravity (x/y/z), bipolar ExG, thermistor, thoracic effort (RIP), abdominal effort (RIP), DC (0-1V) battery, event buttom, SpO2, SpO2B-B, SpO2 quality, pulse rate, plesthymography, RD quality, PPG; + multiple derived channels. Optional proxies add up to 8 EEG, 2 EOG, 3 chin EMG, 2 channels leg EMG and 1 ECG channel 24: (15 recorded channels, 9 derived channels) 2x bipolar channels: RIP, abdomen + thorax breathing effort, respiratory sound, audio volume, gravity, activity, position, flow, snore, PWA; pulse, SpO2; 9 derived: heart rate; calibrated RIP flow, calibrated RIP sum, RIP flow, RIP sum, RIP phase, PTT, respiratory rate 15: EEG right, EEG left, EOG right, EOG left, EMG right, EMG left, SpO2, respiratory effort (via bioimpedance), respiratory flow (via bioimpedance), respiratory flow (via nasal cannula), ECG, activity, body position, sound pressure level, EMG leg 4: peripheral arterial tonometry, pulse rate, oximetry, actigraphy 6: plethysmogram, pulse rate, heart rate variability, respiration, oximetry, actigraphy 6: plethysmogram, pulse rate, heart rate
variability, respiration, oximetry, actigraphy 5: airflow, oximetry, heart rate, chest effort, and respiratory sound (snoring) 11: respiratory airflow, snore, CPAP pressure, thoracic breathing effort, SpO2, pulse rate, finger plethysmogram, body position, movement, patient marker; optional: abdominal breathing effort 7: airflow, heart rate, oximetry, head position, actigraphy, two respiratory effort signals 18: position, airflow, pressure, staging, snoring, effort (abd, thx), SpO2, heart rate, HRV, PPG, temperature (abd, thx), temperature deviation (abd, thx), respiratory rate, movement, background noise
editable autoscored full disclosure signals with forehead-based self-application. For multinight evaluation of sleep
architecture and sleep continuity in home or hospital,
with auto-detection of sleep
biomarkers associated with
neurodegeneration. PSG2 upgrade enables auto-detection of apneas, hypopneas and RERAs, and REM-related SDB severity. 5: Plethysmogram, pulse rate, heart rate variability, oximetry, actigraphy 8: airflow, snore, SpO2, pulse rate, chest effort,
body position, CPAP pressure, PPG 13: thoracic/abdominal effort, pressure, pressure-based
snore, snore sensor, thermistor, SpO2, pulse rate, plethysmography, body position, 3
channels ExG 16: 2x frontal EEG, 2x EOG chin, EMG, nasal cannula, chest and abdomen effort (RIP belt), SpO2, 2-lead ECG (heart rate), pulse 2x, leg EMG, audio, body position 8: heart rate, pulse
oximetry, respiratory airflow (CPAP compatible), RIP belt, snore, body
position, auxiliary (second RIP, thermal airflow, or IDcheck), actigraphy 13: nasal pressure, snoring, CPAP mask pressure, thoracic and abdominal effort, body position, SpO2, pulse rate, plethysmography waveform, signal quality, limb movement (or optional nasal thermistor), 2xEXG (EEG, EOG, EMG, ECG, or off) 9: EEG sleep staging, airflow (cannula or Bi/CPAP interface), Bi/CPAP pressure, respiratory effort (RIP), snore, SpO2, pulse rate, plethysmography, tri-axis body position 13: 2x RIP, pressure
transducer, SpO2, pulse, plethysmography, body position, 2x ExG; 3x DC channels, luminosity sensor 19: pressure, sound, gravity (x/y/z), bipolar ExG, thermistor, thoracic effort (RIP), abdominal effort (RIP), DC (0-1V) battery, event buttom, SpO2, SpO2B-B, SpO2 quality, pulse rate, plesthymography, RD quality, PPG; + multiple derived channels. Optional proxies add up to 8 EEG, 2 EOG, 3 chin EMG, 2 channels leg EMG and 1 ECG channel 24: (15 recorded channels, 9 derived channels) 2x bipolar channels: RIP, abdomen + thorax breathing effort, respiratory sound, audio volume, gravity, activity, position, flow, snore, PWA; pulse, SpO2; 9 derived: heart rate; calibrated RIP flow, calibrated RIP sum, RIP flow, RIP sum, RIP phase, PTT, respiratory rate 15: EEG right, EEG left, EOG right, EOG left, EMG right, EMG left, SpO2, respiratory effort (via bioimpedance), respiratory flow (via bioimpedance), respiratory flow (via nasal cannula), ECG, activity, body position, sound pressure level, EMG leg 4: peripheral arterial tonometry, pulse rate, oximetry, actigraphy 6: plethysmogram, pulse rate, heart rate variability, respiration, oximetry, actigraphy 6: plethysmogram, pulse rate, heart rate
variability, respiration, oximetry, actigraphy 5: airflow, oximetry, heart rate, chest effort, and respiratory sound (snoring) 11: respiratory airflow, snore, CPAP pressure, thoracic breathing effort, SpO2, pulse rate, finger plethysmogram, body position, movement, patient marker; optional: abdominal breathing effort 7: airflow, heart rate, oximetry, head position, actigraphy, two respiratory effort signals 18: position, airflow, pressure, staging, snoring, effort (abd, thx), SpO2, heart rate, HRV, PPG, temperature (abd, thx), temperature deviation (abd, thx), respiratory rate, movement, background noise
7: PAT signal, pulse rate, oximetry, actigraphy, snoring, body position, chest motion
7: PAT signal, pulse rate, oximetry, actigraphy, snoring, body position, chest motion
Features:
AcuPebble SA100 is a small and noninvasive medical device offering a clinically validated home sleep test equivalent to the ambulatory gold-standard (cardiorespiratory polygraph followed by manual specialist interpretation). The AcuPebble system accurately extracts multi-channel information from 2 wireless devices (a neck and a finger sensor) to provide a complete sleep study report. It has received the CE mark in Europe and FDA 510k clearance in the US.
Scientifically-validated and
editable autoscored full disclosure signals with foreheadbased self-application. For multinight evaluation of sleep
architecture and sleep continuity in home or hospital,
with auto-detection of sleep
biomarkers associated with
neurodegeneration. PSG2 upgrade enables auto-detection of apneas, hypopneas and RERAs, and REM-related SDB severity. No need for phone pairing or WiFi. The FDA 510(k) cleared ring & artificial intelligence system measures AHI, sleep stages, and autonomic nervous system response. The cradle allows multiple-night testing (~14 nights) & acts as a digital sleep diary. 7 sizes of changeable ring arms. The web portal allows manual scoring and event editing. Optional smartphone application empowers remote data upload to check if a good study is recorded. Local PC software or the
BridgeBuilder Cloud Portal. SDB analysis including RERA, flow limitation, breath
statistics, SpO2 perfusion.
Carrying case, patient instructional video, USB cable. CPAP compatible, multiple nights, immediate report
access, unlimited custom
reports, locking connectors, stainless steel connector, LED study status indicator, all internal biosensors.
sleep staging technology with
traditional respiratory channels to report an AHI based
on EEG-derived sleep time and body position (not just recording time). With one-touch controls, multi-night
recordings, and a full-color LED interface, the Synergy is now PAP compatible and
backed by a HIPAA-compliant cloud portal.
timed start options; high
resolution screen with signal display; signal test
features (including impedance measurement),
signal quality/status
information; disposable
and reusable sensors
available;
RemLogic or Natus SleepWorks for HST recordings included. The Nox T3s has refined Nox RIP technology with
200 Hz sampling frequency, which can be used as a primary flow measurement;
built-in sensors for snoring, EKG, EMG, and EEG, Bluetooth BLE 5.0 technology extending the battery
life for multinight studies, analysis in Noxturnal Software with artificial intel-
ligence. Indicated for use in patients >2 years old.
Connect sensors for easy application by the patient at home—programmed or manual start. Extensive
analysis and reporting software (1 license). Charging and data transfer simultaneously via USB. CPAP-compatible recordings. Auto
detection of sleep/wake. Additional
abdomen belt available. Also available: SOMNOtouch RESP eco, a Type III and IV home sleep test. The device detects respiratory events such as obstructive and central apneas and hypopneas, respiratory event-related arousal and identifies sleep time, stages, micro-arousals, and position. The device generates sleep parameters, eg, apnea hypopnea index, respiratory disturbance index, oxygen desaturation index, REM and NREM sleep stages, total sleep time, arousal index, % of time spent increased respiratory effort and position. With 18 channels (including 8 FDA-cleared channels), Wesper is a comprehensive sleep management system. Generate autoscored reports with full overscoring capabilities with access to raw data. With this cloud-based system, you can now reduce your cost per patient while giving better care. WatchPAT 300 is simple, accurate, and reliable HSAT that has a smart design to streamline the workflow. It may also utilize screening, pre and post sleep questionnaires through a smartphone app, which helps clinics to streamline diagnostic processes. WatchPAT 300 provides a validated autoscored report and raw data for manual review and editing. The report differentiates obstructive and central events and provides AHI, AHIc, RDI, and ODI based upon TST, and sleep staging.
editable autoscored full disclosure signals with foreheadbased self-application. For multinight evaluation of sleep
architecture and sleep continuity in home or hospital,
with auto-detection of sleep
biomarkers associated with
neurodegeneration. PSG2 upgrade enables auto-detection of apneas, hypopneas and RERAs, and REM-related SDB severity. No need for phone pairing or WiFi. The FDA 510(k) cleared ring & artificial intelligence system measures AHI, sleep stages, and autonomic nervous system response. The cradle allows multiple-night testing (~14 nights) & acts as a digital sleep diary. 7 sizes of changeable ring arms. The web portal allows manual scoring and event editing. Optional smartphone application empowers remote data upload to check if a good study is recorded. Local PC software or the
BridgeBuilder Cloud Portal. SDB analysis including RERA, flow limitation, breath
statistics, SpO2 perfusion.
Carrying case, patient instructional video, USB cable. CPAP compatible, multiple nights, immediate report
access, unlimited custom
reports, locking connectors, stainless steel connector, LED study status indicator, all internal biosensors.
Add Sleep Time to HSAT testing with ApneaTrak:TST or EnsoData integration. Three versions available: Core (Type III), Legacy (AASM-recommended parameters), TST (3xExG channels). Use the same sensors recommended for in-lab studies. Connection to the PC (zero-click) automatically downloads the recording, clears, recharges, and prepares ApneaTrak for the next patient.
Remote upload, autoscoring, Odds Ratio Product sleep depth algorithm. AASM-compliant HST with “Smart Check” green/red light to indicate if a good study was recorded. Uses a RIP belt, CPAP compatible, and can collect multinight studies. Web-based software offers access to studies/scoring/reports, from anywhere facilitating collaboration between sleep labs and physician offices. Service available for manual scoring. Carrying case included, will deliver results while patient is on CPAP, includes video instruction for patient, 24/7 technical support, and analysis, scoring, and reporting software. Designed for basic HST workflow with automated respiratory event analysis and customized reporting. Supports both nasal pressure and thermistor airflow signal. A chest-worn device that combines single-channel EEGsleep staging technology with
traditional respiratory channels to report an AHI based
on EEG-derived sleep time and body position (not just recording time). With one-touch controls, multi-night
recordings, and a full-color LED interface, the Synergy is now PAP compatible and
backed by a HIPAA-compliant cloud portal.
A compact polysomnography type III and IV device powered by one AA battery, the HST Compass contains 2x AC bipolar channels, pressure transducer, integrated RIP interfaces, oximeter, integrated body position and DC channels—all embedded into a single module that will comfortably fit on the chest. Capability to see the traces and study information right on the screen.
Scalable multi-night recorder with auto ortimed start options; high
resolution screen with signal display; signal test
features (including impedance measurement),
signal quality/status
information; disposable
and reusable sensors
available;
RemLogic or Natus SleepWorks for HST recordings included. The Nox T3s has refined Nox RIP technology with
200 Hz sampling frequency, which can be used as a primary flow measurement;
built-in sensors for snoring, EKG, EMG, and EEG, Bluetooth BLE 5.0 technology extending the battery
life for multinight studies, analysis in Noxturnal Software with artificial intel-
ligence. Indicated for use in patients >2 years old.
Onera’s patch-based no-wire STS system records data from up to four contact points, maximizing patient comfort. With their intuitive design, these noninvasive devices are attached within minutes, are easy for patients to use, and save time during hook-up and removal. The user-centric technology offers new opportunities for sleep clinics to expand their programs and for hospitals that have limited or no access to a sleep clinic to implement sleep diagnostic testing within their institution.
A fully disposable device based on peripheral arterial tonometry that provides pAHI and TST estimate. Autoscored reports available in the free NightOwl Portal. Smartphone connected. Device in line with AASM guideline requirements. Reimbursable for qualified physicians. Good for up to 14 nights on 1 patient. The FingerTip is a personalized, single patient use device that comes with three reports generated via the SleepImage software as a medical device (SaMD) cloud based system. Report includes AHI 3% and 4% (OSA and CSA), RDI and ODI based on TST and sleep staging, as well as sleep efficiency, latency, onset, duration, fragmentation, periodicity, NREM and REM sleep, WASO and wake transition. FDA cleared for children and adults. SleepImage generates a report that is ready for interpretation in minutes after a sleep study. Report includes AHI 3% and 4% (OSA & CSA), RDI, and ODI based on TST and sleep staging, as well as sleep efficiency, latency, onset, duration, fragmentation, periodicity, NREM and REM sleep, WASO, and wake transitions. FDA-cleared for children and adults. Service includes auto + RPSGT manual scoring, with differentiation of obstructive and central events. Analyzed indices include count. of apneas, hypopneas, AHI, RDI, REI, CI, ODI, acoustical snoring analysis. Raw data provided in an industry standard format. Resumable recording and rechargeable battery allow easy multi-night testing. Results based upon analyzed sleep time. Plug and play with IntelligentConnect sensors for easy application by the patient at home—programmed or manual start. Extensive
analysis and reporting software (1 license). Charging and data transfer simultaneously via USB. CPAP-compatible recordings. Auto
detection of sleep/wake. Additional
abdomen belt available. Also available: SOMNOtouch RESP eco, a Type III and IV home sleep test. The device detects respiratory events such as obstructive and central apneas and hypopneas, respiratory event-related arousal and identifies sleep time, stages, micro-arousals, and position. The device generates sleep parameters, eg, apnea hypopnea index, respiratory disturbance index, oxygen desaturation index, REM and NREM sleep stages, total sleep time, arousal index, % of time spent increased respiratory effort and position. With 18 channels (including 8 FDA-cleared channels), Wesper is a comprehensive sleep management system. Generate autoscored reports with full overscoring capabilities with access to raw data. With this cloud-based system, you can now reduce your cost per patient while giving better care. WatchPAT 300 is simple, accurate, and reliable HSAT that has a smart design to streamline the workflow. It may also utilize screening, pre and post sleep questionnaires through a smartphone app, which helps clinics to streamline diagnostic processes. WatchPAT 300 provides a validated autoscored report and raw data for manual review and editing. The report differentiates obstructive and central events and provides AHI, AHIc, RDI, and ODI based upon TST, and sleep staging.
WatchPAT ONE is a fully disposable HSAT that also utilizes screening, pre and post sleep questionnaires through a smartphone app, which helps clinics to streamline diagnostic processes. As soon as the study is completed, sleep data is available for interpretation. It provides a validated autoscored report and raw data for manual review and editing. The report differentiates obstructive and central events and provides an AHI, AHIc, RDI, and ODI based upon TST, and sleep staging
