6515--NX EQ Automated Cardiac Resuscitators (VA-26-00023098)

DESCRIPTION

The Veterans Health Administration (VHA) Non-Expendable Equipment National Program has identified the Automated Cardiac Resuscitators product line as a candidate for a VA-wide (otherwise referred to as national ) single Requirements contract award.

The Department of Veterans Affairs (DVA) Office of Procurement, Acquisition and Logistics (OPAL) Strategic Acquisition Center (SAC) on behalf of VHA is issuing this Sources Sought Notice in accordance with the FAR 10.002(b)(2) to determine the availability and technical capabilities of qualified sources.

The SAC in conjunction with VHA is seeking a qualified source to provide Stryker® brand name or equal to the Automated Cardiac Resuscitators on an agency wide basis. VA intends to award a Requirements Contract with Firm-Fixed Price (FFP) orders IAW FAR 16.503, Requirements Contract to a supplier of this equipment. Vendors will be required to deliver the Automated Cardiac Resuscitators to VA medical centers and facilities throughout the United States and its territories.

The anticipated period of performance is for one 12-month base period with four 12-month option periods from the date of award. However, the Government's decision as to whether to continue with the contract, upon annual review, will be based upon successful performance during each previous year and continued need. The Contractor must demonstrate the ability to meet all requirements for the solicitation.

The associated North American Industrial Classification System (NAICS) code for this procurement is 339112- Surgical and Medical Instrument Manufacturing, Product Service Code: 6515 Medical and Surgical Instruments, Equipment, and Supplies and the associated size standard is 800 employees. The FAR Provision found at 52.204-7(b)(1) requires that All interested Offerors must be registered in SAM.gov prior to submitting an offer or quotation. You may access the website at SAM.gov | Home. All offerors must be certified with the appropriate NAICS code on the SAM website. All SDVOSB/VOSB offerors must be verified in the SBA database at: https://veterans.certify.sba.gov/#search at the time of proposal submission.

Submissions for this source sought shall be submitted by email no later than December 18th, 2025, at 10:00am EST to all the following:

Jalima.Jones@va.gov

Sara.Vickroy@va.gov

This notice is for planning purposes only and does not constitute a commitment on the part of the Government to award a contract, nor does the Government intend to pay for any information submitted as a result of this notice. This Sources Sought Notice is part of a continuous process for obtaining the latest information on the commercial status of the industry with respect to their current and near-term abilities. The information provided herein is subject to change and in no way binds the Government to solicit for, or award, a competitive contract. It is emphasized that this is a notice solely for planning and informational purposes.

2.0 SCOPE

Automated Cardiac Resuscitators provide automated chest compressions and are used as a substitute for manual external cardiac compressions during cardiopulmonary resuscitation (CPR). They deliver a more consistent applied force and rate of compression than manual CPR and are designed to relieve rescuers of the exhausting effort of sustained chest compressions and to free them to more effectively manage resuscitation activities. They are designed to artificially produce blood flow in a patient during cardiac arrest. They are pneumatically or electrically driven and apply mechanical compressions cyclically to the sternum or to a wider section of the thorax, causing the heart to eject blood. Automated Cardiac Resuscitators can be used in both the out-of-hospital and in-hospital settings.

The following Contract Line-Items Number (CLIN) are being considered:

CLIN

Manufacturer

Part Number

Description

0001

Stryker

99576-000063

Lucas® 3, v3.1 Chest Compression Device Includes:

Hard Shell Case

Slim Back Plate

2 Patient Straps

Stabilization Strap

Suction Cups

1 Rechargeable Battery

Instructions for Use with Each Device

0002

Stryker

11576-000080

Battery - Rechargeable

0003

Stryker

11576-000060

Battery Charger - Desktop

0004

Stryker

11576-000090

Grip Tape (3-pack) for Slim Back Plate

0005

Stryker

11576-000047

Suction Cups - Disposable (12-pack)

0006

Stryker

99576-000042

Training Device

0007

Stryker

11576-000050

LUCAS Patient Straps

0008

Stryker

21576-000074

LUCAS Stabilization Stap

0009

Stryker

11576-000051

LUCAS Patient Straps (3-pack)

0010

Stryker

11576-000046

LUCAS Suction Cup (3-pack)

0011

Stryker

21576-000075

LUCAS Stabilization Strap (4-pack)

0012

Stryker

11576-000071

LUCAS Power Supply

0013

Stryker

11576-000094

LUCAS Hard Shell Carrying Case

0014

Stryker

11576-000088

LUCAS Back Plate Standard

0015

Stryker

11576-000064

LUCAS Back Plate Carbon Fiber

0016

Stryker

11576-000080

LUCAS 3.0/3/1 Battery

0017

Stryker

11576-000048

LUCAS Car Cable

0018

Stryker

11576-000060

LUCAS Battery Desktop Charger

0019

Stryker

11576-000053

Back Plate Grip Tape (3-Pack)

The Department of Veterans Affairs (VA) is seeking vendors who can provide Stryker® brand name or equal Automated Cardiac Resuscitators as listed above or equal commodities which meet all the following salient characteristics (SCs):

SC #

SALIENT CHARACTERISTICS

Applicable CLIN

METHOD OF EVALUATION

SC 1

Compressions Per Minute 100-120

0001, 0002, 0003, 0005

Literature Review

SC 2

Compression Depth cm (in) 5cm (2in)

0001, 0005, 0006

Literature Review

SC 3

Transfer Time from Manual CPR 10 Seconds

0001, 0006

Literature Review

SC 4

Patient Weight: Must operate with patients weighing more than 300lbs (136kg)

0001, 0006

Literature Review

SC 5

Patient Chest Width: Must operate with patients that have a chest width up to 44.9cm (17.7 in)

0001, 0006

Literature Review

SC 6

Patient Sternum Height: Must operate with patients that have a chest height up to 30.3 cm (11.9 in)

0001, 0006

Literature Review

For each product (brand name and part number), the response must include descriptive literature demonstrating the product meets or exceeds the salient characteristics specified above.

The Government's intent is to include all ancillary items to ensure the equipment can function as designed by the Original Equipment Manufacturer (OEM) and as clinically required. Vendors are encouraged to provide any product solution or configuration so long as they meet the salient characteristics. Additionally, responses can include any additional product that may be beneficial. These items must be clearly identified by brand name and part number.

Responses to this Sources Sought Notice shall include the following:

Does vendor offer an annual service plan, Yes or No?

If Yes:

What does the plan cover?

Does plan cover software updates only?

Does the plan cover parts repair or replacement only?

Does the plan cover both software and parts?

Vendors are requested to provide documentation that shows information on their service plan.

Is the service provided by the OEM or a subcontractor?

Full name and address of company

CAGE Code/ SAM UIE

Business Size

Manufacturer or Distributor

If the distributor provides full name, business size and address of manufacturer.

Country of Origin designation for all products

Ability to provide uninterrupted supply of products on a national scale.

Technical Literature that clearly shows product(s) meets the identified salient characteristics and page numbers where each salient characteristic is met.

Any additional product solution or configuration that would be beneficial to the clinical functionality of the product line identified.

Authorized Distributor Letter Certified by OEM with a current date.

Although not required, vendors responding to this Sources Sought may also submit a Capabilities Statement.