DOCUMENT
65 -- Sleep Monitoring System - Attachment
- Notice Date
- 4/13/2017
- Notice Type
- Attachment
- NAICS
- 334510
— Electromedical and Electrotherapeutic Apparatus Manufacturing
- Contracting Office
- Kim Pauley;Department of Veterans Affairs;Network Contracting Office 6;100 Emancipation Drive;Hampton VA 23667
- ZIP Code
- 23667
- Solicitation Number
- VA24617N0833
- Response Due
- 4/18/2017
- Archive Date
- 7/2/2017
- Point of Contact
- Kim Pauley
- E-Mail Address
-
kim.Pauley@va.gov
(kim.Pauley@va.gov)
- Small Business Set-Aside
- Service-Disabled Veteran-Owned Small Business
- Description
- This is a sources sought for a NOX-T3 Portable Sleep Monitor Device and Nocturnal Software. The equipment is brand name or equal, see list below for salient characteristics. To be considered to receive a solicitation for quote please submit a product brochure for clinical consideration as an equal product if it is not brand name. This is not a solicitation, responses to this notice will be used as Market Research only. Please respond to kim.pauley@va.gov no later than April 18, at 11:00 AM EST if your company can supply this product. Please provide your Dun and Bradstreet number and socio-economic status if you are interested in this contract. It is the intent of the government to solicit and award this contract if possible to an SDVOSB. Carefully consider the brand name or equal product prior to submitting your interest in this contract. Items Include: QTY U OF M DESCRIPTION 50 EACH 22857-001 NOX T3 COMPLETE KIT,US VERSION Portable sleep monitoring system: Digital recorder, 2 respiratory effort sensors, clip straps, USB cable, abdomen thorax cable, filter tube connectors, batteries and software for communication with the device, analyzing and reviewing of data. Standard 2 year replacement warranty. Storage capacity 1GByte, Recording time greater than 24 hours including true audio recording; PC communications USB 2.0 Hi-Speed; Power Source 1 1.5V AA battery during recording; Battery Type - Alkaline primary, Nickel-metal hydride rechargeable (NiMH); Internal Signals Thorax and Abdomen RIP Respiratory Effort + RIP Flow, Flow Pressure/CPAP pressure, Snore, Audio recording channel 2x bipolar channels (EMG, ECG, EEG, etc.), Position, Activity; Flow/Pressure signal 25cmH2O input pressure range DC-90Hz, less than 2mmH2Orms noise; RIP signals 2 channels; Activity/position signals Internal 3 axis, ?6g; Sound signals Internal 3.8kHz Bandwidth, 16-bit ADC; Wireless External Signals SpO2, Pulse, Plethysmograph, SpO2 quality; Wireless Interface Bluetooth V2.0 Wireless interface with Nonin oximeters. Device Dimension 79mm (3.11") W, 63mm (2.48")H, 21mm(0.83") D; Weight 65 gram (88 gram with battery); Display Type OLED 1 EACH 97075-ADV-SLP SLEEP 1-DAY ONSITE ADVANCED APPLICATIONS Sleep 1-day Onsite advanced applications in conjunction with Operator training course. SALIENT CHARACTCARACTERISTICS NOX-T3 Portable Sleep Monitor device and Noxturnal software REQUIRED SPECIFICATIONS The device shall be capable of delivering the processed signals 2x RIP channels, RIP SUM, RIP Flow, RIP phase, Nasal pressure, Snore from nasal pressure, Audio Intensity, Audio Playback, Position, Activity, SpO2, HR (pulse rate), pleth wave form, 2 Aux channels for AC sensor input (EEG, EKG, EOG, limb movement, thermistor, bruxism), pulse transit time, and blue tooth end tidal CO2 number and waveform. The device shall be rated for adult and pediatrics from 2 years of age and older. The device software shall be capable of bidirectional connection to the EHR through a gateway. The device software shall be capable of complete PSG scoring capability. The device shall use blue tooth technology for collection of pulse oximetry, HR, and peth waveform. The device shall have a small form factor and be light weight. Device shall weigh (battery included) less than 150 g. Device dimension height and width shall be less than 10 cm. Device thickness shall be less than 3cm. The device shall measure respiratory movements on the abdomen and thorax using RIP technology. The respiratory belt signal shall cover the patient range from 30cm to 210cm circumference and shall show the respiratory movements for both shallow and extreme breathing in that range. The device shall measure the patient s body position and activity. The device shall measure nasal pressure by use of a nasal cannula. The device shall be capable to measure temperature by thermistry. The device shall have an inbuilt microphone for recording of sounds and measure sound intensity. The sound signal shall be sensitive enough to function accurately even when positioned under a comforter. The device shall allow the reporting of snoring sounds in adults and pediatrics in the unit of dB. The device shall be able to measure and deliver signals continually for at least 8 hours using commercially available batteries. The device shall operate on standard replaceable batteries. The recorder shall tolerate routine clinical cleaning with isopropyl alcohol. The device shall have mini-USB connector for connection to a PC. The device shall have on-board display, used to display information on device status and live signal status during hookup. The device shall have on-board buttons, used to control the device and control information shown on the device s display (scroll through display pages). The device shall be able to connect to any standard nasal cannula with male luer connector for measurement of airflow. The battery compartment shall be child proof. The device shall be capable of transferring its data to EDF (European Data Format). The device shall be capable of auto scoring immediately after study completion. The device shall be capable of auto-start and auto-stop for successive days with set up within the software using a standard built-in calendar. The device software shall be able to share the same EHR gateway with other CareFusion respiratory diagnostic products. The device software shall have wizards for viewing existing recordings, starting a new recording, and downloading and viewing recordings. The device software shall be capable of storing the studies either locally or on a network drive. The device software shall be able to auto save workspace. The device software shall be able to be used for both US and metric settings with mouse click change. The device software shall be able to browse and set default data location. The device software shall allow for default analysis protocols to be used and allow for creation of custom analysis protocols. The device software shall allow for set up for notch filters. The device software shall be able to open a new score set, and save multiple score sets on the same patient. The device software shall be able to adjust/revert adjust/change scoring that is already done. The device software shall be able to make custom reports including diagnostic, treatment, and comparison reports for both adult and pediatrics. The device software shall be able to use current AASM guidelines for scoring for both pediatrics and adults. The device software shall be able to present user with a dashboard for the study of the entire night. The device software shall be able to adjust beginning and end of study with drop and drag feature on hipnogram. The device software shall be able to use tabs as pages to view all raw signals and utilize drag-and-click scoring. The device software shall be able to stage sleep. The device software shall be able to create and use canned textual interpretative statements and place into interpretation with a mouse click. The device shall come with a standard 2-year warranty. The device shall offer additional year s warranty at discounted rate when purchased up front with device sale.
- Web Link
-
FBO.gov Permalink
(https://www.fbo.gov/spg/VA/HaVAMC/VAMCCO80220/VA24617N0833/listing.html)
- Document(s)
- Attachment
- File Name: VA246-17-N-0833 VA246-17-N-0833.docx (https://www.vendorportal.ecms.va.gov/FBODocumentServer/DocumentServer.aspx?DocumentId=3414028&FileName=VA246-17-N-0833-000.docx)
- Link: https://www.vendorportal.ecms.va.gov/FBODocumentServer/DocumentServer.aspx?DocumentId=3414028&FileName=VA246-17-N-0833-000.docx
- Note: If links are broken, refer to Point of Contact above or contact the FBO Help Desk at 877-472-3779.
- File Name: VA246-17-N-0833 VA246-17-N-0833.docx (https://www.vendorportal.ecms.va.gov/FBODocumentServer/DocumentServer.aspx?DocumentId=3414028&FileName=VA246-17-N-0833-000.docx)
- Record
- SN04471989-W 20170415/170413235236-6db6fdf1a15d8be5ea1b8b23131023b9 (fbodaily.com)
- Source
-
FedBizOpps Link to This Notice
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