Redacted LSJ- VHP Sterilzer Evans Army Community Center
Updated
A PDF document (171 KB) attached to Hospital Supply Division, from the Defense Logistics Agency.
File name: Redacted LSJ- VHP Sterilzer Evans Army Community Center.pdf
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LIMITED SOURCES JUSTIFICATION (LSJ)
(1.) Defense Logistics Agency (DLA) Troop Support, Medical Supply Chain, Hospital Supply Division is the contracting activity.
(2.) The justification is for the acquisition of the three (3) Vaporized Hydrogen Peroxide (VHP) Sterilizers as required by Evans Army Community Hospital (EACH) Fort Carson. The order will be placed under Equipment ECAT Solicitation SPE2DH-21-R-0002; contract SPE2DH-24-D-0011, which is valid through May 15, 2029.
(3.) The acquisition is for the purchase of the following items for EACH: Item Description: Vaporized Hydrogen Peroxide (VHP) Sterilizer Manufacturer: Steris
Manufacturer Part Number (P/N): VP50002101
Quantity: 3/EA
Unit Price:
The total estimated dollar value of this action is
(4.) The authority waiving the competition requirements is FAR 8.405-6(a)(1)(i)(B), only one source is capable of providing the supplies or services required at the level of quality required because the supplies or services ordered are unique or highly specialized. The use of this authority is necessary to meet EACH’s requirements for low-temperature medical VHP Sterilizers. EACH requires this equipment for use within the medical center’s Sterile Processing Department (SPD). This device is necessary to sterilize medical equipment, control infection and prevent disease transmission.
The required VHP Sterilizer must satisfy all of the following minimum requirements established by
EACH:
a. Freestanding or Recessed Dimensions and Voltage Configuration – The device shall have a configuration that is freestanding or recessed and shall fit into EACH’s current SPD footprint. The device shall fit into the following dimensions: Cabinet: 33X40-15 / 16 X 72”, Recessed/Cabinet: 33X38-5 / 16 X 72”, Shelf clearance: Top- 6-15/16”, Bottom- 7-1/16”. The device shall be fully functional utilizing a standard electrical power connection that can withstand voltage fluctuations. b. FDA Clearance—The device shall be cleared by Food and Drug Administration for terminal sterilization of medical devices.
c. Material Compatibility & Capability – The device shall be capable of sterilizing temperature sensitive tools and equipment currently in use at EACH including but not limited to scopes, in particular DaVinci Scopes, cameras, and light cords.
d. Hydrogen Peroxide Sterilant – The device shall use vaporized hydrogen peroxide as a sterilant. e. No Presence of Plasma, Chamber Temperature – The device shall sterilize heat-sensitive
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