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FBO DAILY - FEDBIZOPPS ISSUE OF FEBRUARY 22, 2015 FBO #4838
DOCUMENT

61 -- SonoSite EDGE - Attachment

Notice Date
2/20/2015
 
Notice Type
Attachment
 
NAICS
334510 — Electromedical and Electrotherapeutic Apparatus Manufacturing
 
Contracting Office
Department of Veterans Affairs;Network Contracting Office 20;5115 NE 82nd Ave, Suite 102;Vancouver WA 98662
 
ZIP Code
98662
 
Archive Date
4/21/2015
 
Point of Contact
Traci R Jackson
 
E-Mail Address
2-9897<br
 
Small Business Set-Aside
N/A
 
Description
The Department of Veterans Affairs, VISN 20, in accordance with FAR 13.106-1(b)(1) (single source), intends to negotiate on a sole source basis with SONOSITE INC for the following ultrasound-imaging equipment listed below. NAICS 334510 applies. This notice of intent is not a solicitation or request for offers. No solicitation package is available. All responsible sources may submit a capability statement, proposal, or quotation which shall be considered. A determination not to compete is solely within the discretion of the Government. Any response to this notice must show clear and convincing evidence that the responding company can provide ultrasound-imaging equipment with all specifications listed below. Responses must be received no later than 4:30 pm on February 26, 2015. All responses must be e-mailed to Traci.jackson1@va.gov The equipment must be capable of operating in B Mode, M-Mode, Color Doppler, Color Power Doppler (CPD), Pulsed Wave and Continuous Wave modes. It must support transducers with linear, phased array and curved array formats. Further, it must include a full array of measurement and calculation packages. The specific requires for this equipment are the following: 1.System Design Requirements a.The system shall include a digital beamformer with the ability to transmit, receive and process acoustic data from up to 128 transmit channels and 64 receive channels. Multi-plexing should be available for use in the transducer to connect the channels to array's currently with up to 256 elements. Synthetic aperture shall be utilized to expand the receive aperture to improve lateral resolution in multiples of 64 channels per acoustic firing. b.The system shall include a digital beamformer with a 128 element transmit aperture. c.The system beamformer shall use 64 analog to digital converters. d.The system shall have broadband architecture with an operating frequency of at least 1 to 15 MHz. e.The system shall process a dynamic range that is at least 165db f.The system shall support a gray scale range of 256 levels, 8 bits. g.The system shall provide a backlit keypad for ease of use. h.The system shall have the ability to function by AC/DC or battery power with the same degree of functionality. i.The system shall go from the off status to active scanning in fewer than 20 seconds. j.The system shall support ECG. k.The system shall be able to be hand carried. l.The system shall be able to withstand a drop from a height of 36 inches onto a steel plate and remain safe. m.The system shall weigh no more than 3.9 kg / 8.5 lbs. n.The system shall be no larger than 32.77 cm (L) x 31.5 cm (W) x 16.26 cm (D) / 12.9" (L) x 12.4" (W) x 6.4"(D). o.The system shall have an LCD screen size no smaller than 12.1" p.The system display area shall be no smaller than VGA 246.0 (H) x 184.5 (V) mm q.The system display contrast shall be 900:1. r.The system display brightness (luminance) At IL=50mA/One circuit 450 cd/msq (typ) s.The system display-viewing angle shall be at least 80 ° left to right. t.The system shall have Digital Video Interface (DVI), S-Video, and audio output via an optional docking system. u.The operating temperature range of the system, transducers, and battery shall be 10-40 °C. v.The operating altitude of the system, transducer, and battery shall be up to 3000m (9800 ft). w.The operating humidity range of the system, transducer, and battery shall be 15-95%. x.The storage and shipping temperature range of the system and transducer shall be -35 -65 °C. y.The storage and shipping temperature range of the battery shall be -20 -60 °C. z.The storage and shipping altitude of the system shall be up to 5500m (18,000 ft). aa.The storage and shipping humidity range of the system, transducers, and battery shall be 15-95%. bb.The battery life (run time) shall be up to 2 hours. The time to charge the battery to full capacity shall be 4 hours with a battery shelf life of 60 days. 2.Measurement and Analysis a.The system shall provide the user with generic digital calipers. b.The system shall support up to 8 generic distance calipers. c.The system shall provide the user with up to 4 generic trace tools. d.The system shall provide the user with up to 4 generic ellipse tools. e.The system shall provide the user with a generic heart rate tool. f.The system shall provide a generic pressure half time tool. g.The system shall provide a hip angle measurement tool. h.The system shall have a dedicated obstetrical calculations package. i.The system shall have a dedicated vascular calculations package. 3.B-Mode/ M-Mode Imaging a.The system shall provide the user with controls for optimizing resolution in B-Mode. b.The system shall display at a maximum depth of 35 cm, and a minimum of 1.5 cm. c.The system shall provide a timeline Cine function with at least 200 frames of available review. d.The system shall support frame rates up to 60Hz in 2D. e.The system shall provide the user with at least seven-user selectable post processing / dynamic range gray scale maps. f.The system shall have the ability to transmit from one frequency and receive at a higher harmonic frequency to reduce noise and clutter, and improve image. g.The system shall have the ability to enhance tissue margins and improve contrast resolution by reducing artifacts and improving visualization of texture patterns within the image. h.The system shall provide the user with a zoom function that increases the region of interest. i.The system shall allow the user to scan with at least three simultaneous focal zones in B-Mode in order to maximize gray scale resolution. j.The system shall provide the user with the ability to flip the image horizontally and vertically. k.The system shall provide a dual multi-image function on a single monitor with the ability to individually scan the images on each side. l.The system shall provide a dual multi-image display function with all transducers that positions the two displays along side each other in a seamless fashion for ease of visualizing an extended field of view from two separate scan positions. 4.Color and CPD a.The system shall include a non-directional color power mode (CPD). b.The system shall provide velocity color Doppler. c.The system shall support a color frequency range of 106 - 29,762 Hz. d.The system shall provide a user controlled mechanism to easily control the size and position of the Color/CPD Region of Interest (ROI) including independent control of its height and width. e.The system shall provide the user with controls for optimizing resolution in Color modes. f.The system shall provide the user with a scale control that varies the scale range in color. g.The system shall provide the user with at least three-user selectable wall filter options. h.The system shall have velocity color flow imaging, providing the clinician with the color sensitivity to perform color Doppler examinations with all transducers during a clinical procedure. 5.Doppler a.The system shall provide Pulsed Wave (PW) Doppler mode. b.The system shall provide Tissue Doppler Pulsed Wave Doppler (TDI PW) Mode. c.The system shall provide Continuous Wave (CW) Doppler Mode. d.The system shall support quantitative assessment of blood flow with Duplex imaging. e.The system shall have at least 256 gray levels in the spectral display. f.The system shall support a Doppler frequency range of 325 - 40 KHz. g.The system shall provide the user with control during timeline replay to review the spectrum. h.The system shall provide the user with a scale control that varies the scale range. i.The system shall provide the user with at least three-user selectable wall filter options. 6.Image Storage, Archive and Networking a.The system shall have archive capability for storage and retrieval of images and clips. b.The system shall provide the capability to storing clips via time or heartbeats. c.The system shall provide the capability to store clip data prospectively or retrospectively. d.The system shall provide the ability to preview clips prior to committing them to storage. e.The system's storage capacity shall accommodate up to 8GB. f.The system shall be DICOM 3.0 compliant. g.The system shall support the following DICOM functionality, as a minimum: Storage, Print, and Work List. h.The system shall be capable of transferring images by batch or as exam is in progress to a DICOM archive. i. The system has easy to use configuration menus for all networking features. j.The system allows for saving the DICOM configuration via USB so they are easy to replicate or restore. k.The system shall allow for location specific connectivity configuration. l.The system shall provide a comprehensive set of tools that the customer can use for HIPAA Compliance. m.The system shall provide user customizable login and password for up to 20 users. n.The system shall provide a guest login. 7.Transducers a.The transducers shall operate at frequencies from a minimum of at least 1.0 MHz to a maximum of at least 15.0 MHz. b.Transducers shall have biopsy guide capability when applicable. c.Transducers supported by this system will include an L25x / 13-6 MHz multi-frequency, broadband, 25 mm linear array transducer for vascular, musculoskeletal, nerve and superficial imaging. d.Transducers supported by this system will include an L38x / 10-5 MHz multi-frequency, broadband, 38 mm linear array transducer for small parts, breast, vascular, musculoskeletal, nerve and superficial imaging. e.Transducers supported by this system will include an HFL38x / 13-6 MHz multi-frequency, broadband, 38 mm linear array transducer for small parts, breast, vascular, musculoskeletal, nerve and superficial imaging. f.Transducers supported by this system will include a C60x / 5-2 MHz multi-frequency, broadband, 60 mm curved array transducer for general purpose, abdominal, gynecological and obstetric imaging. g.Transducers supported by this system will include an ICTx / 8-5 MHz intracavitary curved array broadband 11mm transducer for intracavitary gynecologic and obstetrical imaging. h.Transducers supported by this system will include a P21x / 5-1 MHz multi-frequency, broadband 21 mm phased array transducer for cardiac, abdominal, and obstetrics imaging. i.Transducers supported by this system will include a C11x / 8-5 MHz multi-frequency, broadband 11 mm curved array transducer for abdominal, nerve, neonatal, and vascular imaging. j.Transducers supported by this system will include HFL 50xi / 15-6 MHz multi-frequency broadband 50mm linear array for musculoskeletal, nerve, breast and superficial imaging. k.Transducers supported by this system will include Multi-plane TEE / 8-4 MHz multi-frequency broadband transducer for transesophageal imaging. l.Transducers supported by this system will include an SLA / 13-6 MHz multi-frequency broadband transducer for vascular, venous, and small-parts imaging. 8.Accessories a.An optional mobile docking station shall be available to store and/or transport the system. b.The mobile docking station shall have an option for at least three active transducer ports in a convenient to access location. c.The mobile docking station shall have an adjustable height keyboard. d.The system shall be able to be connected to external peripheral devices such as an external monitor, printer, and/or DVDR. e.The system shall be able to be connected to an optional footswitch for hands-free operation. f.The system shall have as an option a cordless charging option. g.The system shall have an additional fixed battery option to expand the battery life x 2. 9.Service a.The manufacturer shall provide toll free service support help. b.The manufacturer shall provide a five-year standard warranty on the system. c.The manufacturer shall provide a five-year standard warranty on transducers, excluding the multi-plane transesophageal and surgical transducers. d.The manufacturer shall provide a one-year standard warranty on the multi-plane transesophageal and surgical transducers. e.The manufacturer shall provide a one-year standard warranty on accessories carrying the manufacturer's label excluding the system battery (6 months). f.The manufacture shall provide a loaner system within 24hrs where available (24 hr shipping not available in all geographical locations).
 
Web Link
FBO.gov Permalink
(https://www.fbo.gov/notices/d05f70dc6137db81ba197f05bfbc0e58)
 
Document(s)
Attachment
 
File Name: VA260-15-P-1677 VA260-15-P-1677.docx (https://www.vendorportal.ecms.va.gov/FBODocumentServer/DocumentServer.aspx?DocumentId=1877626&FileName=-5317.docx)
Link: https://www.vendorportal.ecms.va.gov/FBODocumentServer/DocumentServer.aspx?DocumentId=1877626&FileName=-5317.docx

 
Note: If links are broken, refer to Point of Contact above or contact the FBO Help Desk at 877-472-3779.
 
Record
SN03647302-W 20150222/150220234434-d05f70dc6137db81ba197f05bfbc0e58 (fbodaily.com)
 
Source
FedBizOpps Link to This Notice
(may not be valid after Archive Date)

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