630B50014 _ XR US VAMC NEW YORK NY_ Tech Specification.docx

DOCX document 261 KB Posted

Attached to
6525--DEC 2024 Equipment Only Consolidation Federal contract opportunity
Solicitation number
36A79725Q0003
Issued by
Department of Veterans Affairs National Acquisition Center

About this file

This is a technical specification document for an Ultrasonic (XR US) scanning system required by the VA New York Harbor Healthcare System's Anesthesia Service at their Manhattan Campus. The requirement is to replace one existing cardiac ultrasound unit that is nearing end of life.

The specification calls for one system with a minimum 21-inch screen, 180-degree monitor rotation, 4 transducer ports, and specific size/weight limitations. Key technical requirements include 2D/3D scanning capabilities, multiple Doppler modes, and various analysis packages for vascular and cardiac functions. The system must include five specific transducers (two transesophageal, one transthoracic, one linear array, and one non-imaging Doppler). Additional requirements include DICOM compatibility, wireless connectivity with FIPS 140-2/3 compliance, PACS compatibility with AGFA and VA VistA Imaging, on-site clinical training for 5 technologists and 5 physicians, and a minimum one-year warranty with parts and labor. A Philips Healthcare Epiq 7 (Serial: US914B0953) is available for trade-in consideration.

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Text version

Equipment Specifications Scanning Systems: Ultrasonic (XR US)

V02 NEW YORK NY

XXXBXXXXX

REQUIREMENT OVERVIEW

The VA New York Harbor Healthcare System’s Anesthesia Service currently has one Cardiac Ultrasound at the Manhattan Campus which is nearing end of life. Replacing this equipment will improve overall image quality and improved performance when analyzing echo images during cardiac cases.

Facility Name
New York Harbor Healthcare System
Delivery Address
423 East 23rd St, New York, NY 10010
Requesting Department(s)
Anesthesia
Quantity
1

technical requirements Unit physical specifications

a. Minimum screen size [in]
21
b. Minimum monitor rotation [degrees]
180
c. Minimum number of transducer ports
4
d. Maximum equipment dimensions (HxWxD) [in]
68x24x44
e. Maximum equipment weight [lbs]
105

Scanning modes

☒
a. Two-dimensional (2D)
☒
b. Three-dimensional (3D) – freehand
☒
c. Tissue Harmonic Imaging
☒
d. M-Mode
☒
e. Velocity Color Doppler
☒
f. Color Power Doppler
☒
g. Tissue Doppler Imaging

Doppler displays

☒
a. Frequency
☒
b. Velocity

Control panel specifications

☒
a. Physical keyboard
☒
b. Touchscreen monitor

Additional specifications

☒
a. Panoramic mode
☒
b. Ability to create patient worklist without order or network connection
☒
c. Ability to enter standby mode or sleep mode

Analysis packages

☒
a. Vascular – measurement and analysis of vessels
☒
b. Cardiovascular Clinical
☒
c. Cardiac 3D Quantification

Vendors must include in their offers analysis packages that meet the criteria above. Please include all other analysis packages offered by your company in the optional section on the quotes.

Transducers

Description
Qty
Frequency Range [MHz]
a. Transesophageal
1
8-2
b. Transesophageal
1
11-4
c. Transthoracic
1
5-1
d. Linear Array
1
15-7
e. Non-imaging Doppler
1
2

Vendors must include in their offers transducers that meet the criteria above. Please include all other transducers offered by your company in the optional section on the quotes.

Advanced features

☒
a. Image storage for any captured images

Security/Connectivity requirements

☒
a. OEM-supported operating system
☒
b. Latest DICOM print, store, commit, structured report (SR) and modality worklist
☒
c. Wireless connectivity to VA network – Compatible with 802.11b/g/n and FIPS 140-2 or FIPS-3 compliant
☒
d. Encrypted hard drive
☒
e. PACS compatibility – AGFA
☒
f. PACS compatibility – VA VistA Imaging

training requirements Clinical Training

☒
a. On-site clinical applications training for [5] technologists during go-live
☒
b. On-site follow-up clinical applications training for [5] technologists once technologists have hands-on experience with the system
☒
c. On-site clinical applications training for [5] physicians during go-live
☒
d. Technologists who complete the clinical applications training shall receive continuing education credits (CMEs).
☒
e. Vendors shall be responsible for accommodating different personnel shifts for clinical applications training during go-live.

Biomedical Technician Training Please reference the “Instructions to Offers” for further information about the type of information to provide by equipment type not by specific request. Please also reference the “Instructions to Offers” for response format.

Technical training information to include detailed information about the curriculum and length of the biomedical technical training required for each equipment type.

Although the NAC will not award this training along with the equipment, it is imperative that the customer is informed that this training is available. Vendors must demonstrate that they can provide any required off-site training, therefore off-site training should be quoted as an optional item. Off-site training will be purchased at the time of need via a modification (if the original order remains open) or via a separate order. No travel expenses for any VA employees will be included in any HTME equipment or training order.

service requirements

1. VPN/Remote Access – The vendor shall provide any and all equipment service programs, such as remote diagnostics, during the warranty period. The vendor shall provide post-warranty remote diagnostic service program as an “Add Option” with the offer. The system shall provide vendor remote diagnostics via VPN. The vendor shall either utilize the VA national site-to-site VPN or work with the Office of Cyber and Information Security and the VAMC Information Systems Security Officer to establish a client-based VPN.

2. Service and Operator Manuals – The vendor shall provide the following documentation for the proposed systems:

a. Two (2) copies of operator instruction manuals (one (1) electronic and one (1) physical copy)

b. Two (2) copies of a service manuals (one (1) electronic and one (1) physical copy) *Vendors can include the physical copy as a priced line item in their quote as applicable.

3. Minimum Warranty – The system and accessories shall be covered under the manufacturer’s warranty and shall include all parts and labor for one year following acceptance by the VAMC. This warranty must include PMs as required by the manufacturer. The manufacturer’s factory-trained field service representatives shall perform installation and maintenance during the warranty period.

Vendors are encouraged to include any offerings for service, warranty, and training that may exceed the minimum requirements, to include information on their service support structure during and after the warranty period. Vendors who do not include any added value offerings for service, warranty, and training will not be docked or excluded from consideration. However, any such offerings will be evaluated based on added value.

Added Value Specifications listed below are not required, but preferred. Vendors who do not include the below specifications in the submitted offer will not be docked or excluded from consideration. Specifications listed below will be evaluated based on added value.

☒
a. Additional year(s) of warranty
☒
b. Post-warranty remote diagnostic service program
☒
c. Version/platform long-range plan

other information/documentation requested Please reference the “Instructions to Offers” for further information about the type of information to provide by equipment type not by specific request. Please also reference the “Instructions to Offers” for response format.

1. Completed pre-procurement assessment form (6550 Appendix A)

2. Completed Manufacture Disclosure Statement for Medical Device Security (MDS2) form

3. Federal Information Processing Standard (FIPS) 140-2 or (FIPS) 140-3 certification

4. Product brochures

5. Technical specification sheets, to include dimensions and weight of the system

6. Typical drawings (pdf version of the CAD drawings)

7. Technical training- Biomedical: information to include detailed information about the curriculum and length of the biomedical technical training required for each equipment type.

· Although the NAC will not award this training along with the equipment, it is imperative that the customer is informed that this training is available. Vendors must demonstrate that they can provide any required off-site training, therefore off-site training should be quoted as an optional item. Off-site training will be purchased at the time of need via a modification (if the original order remains open) or via a separate order. No travel expenses for any VA employees will be included in any HTME equipment or training order.

8. Support information to include your company’s support structure during and after the warranty period

· On-line or telephonic applications support and availability (include third party coverage)

· A listing of field service engineer locations and availability

· A listing of part depots trade-in

☒
1. In instances where sanitization of ePHI compromises the OS and/or application software, or requires the removal of internal storage media, the vendor accepts the equipment “as is” and can elect at their own discretion to contract with the original equipment manufacturer (OEM) to restore the system.

The following equipment is available for trade-in. Please reflect any credits provided for trade-in equipment in the proposal.

Station
New York Harbor Healthcare System – Manhattan Campus
Manufacturer
Philips Healthcare
Model
Epiq 7
EE/Asset Number
EE 37978
Serial Number
US914B0953
Current Condition
Operational
Installation Date
OCT 14, 2014
☒
a. VA has no ancillary equipment to offer.

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