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COMMERCE BUSINESS DAILY ISSUE OF JANUARY 12,2000 PSA#2514311th HSW/PKRH, 7909 Lindbergh Drive, Brooks AFB, Tx 78235-5352 65 -- REQUEST FOR INFORMATION (RFI) SYNOPSIS ANNOUNCEMENT FOR THE
COMMERCE BUSINESS DAILY: MEDICAL EQUIPMENT, AEROMEDICAL EVACUATION,
OXYGEN GENERATING SYSTEMS, COMPRESSORS, CRYOGENICS SOL F41624-99-R-1002
DUE 021100 POC Lt John D. Del Barrio, (210)536-2390, Michael J.
Nannery, (210)536-4559, or Capt Bill Schum, (210)536-2367 WEB: RFP Not
Applicable, UNDER CONSTRUCTION. E-MAIL: To contact Contract Manager,
see E-mail address above., john.delbarrio@brooks.af.mil. This is not a
notice of solicitation. The 311th Human Systems Wing at Brooks AFB is
seeking information on the commercial capabilities and costs of
medical equipment, technologies or systems that support the Air Force
Medical Service mission, which provides Patient Therapeutic quality
oxygen in Aeromedical evacuation (AE) aircraft (C-5, C-130, KC-10, and
KC-135). Background -- The current system used to support patient
oxygen requirements in the Air Force Aeromedical evacuation system
(AES) is the Patient Therapeutic Liquid Oxygen System (PTLOX). This
system depends upon the availability of liquid oxygen (LOX) and is
labor intensive to support and maintain. Changes in aircraft oxygen
systems from LOX dependent systems to On-Board Oxygen Generating
Systems (OBOGS), as well as changes in operational employment of forces
has made it increasingly difficult to find LOX to support the PTLOX
systems in forward deployed areas. Additionally, as fewer airframes
depend upon LOX, the ability to maintain these systems in garrison and
while deployed continues to diminish. Unlike the PTLOX system, current
OBOGS do not provide 93-100 percent oxygen. Integration of OBOGS into
existing airframes easily meets flight crew oxygen requirements;
however, certain patient conditions, as well as international standards
for patient care, requite the availability of 93-100 percent oxygen for
therapeutic purposes. Currently, improved oxygen system components and
packaging are needed that will directly meet AES and airlift power,
weight, and size constraints, and deliver 93-100 percent oxygen to
satisfy operational requirements. Information on technologies that
support on-board oxygen generation is being sought. In relation to the
provision of on-board AES missions, either of two (2) separate
concepts of operation is acceptable. (1) A Single piece system that has
the capability to produce, store and deliver therapeutic oxygen in a
single, integrated system that is man-portable and capable of
integration onto all current and potential airframes used in fixed-wing
patient evacuation. Equipment should have the following
characteristics: (a) Human factors: portable, compact, and compatible
with use in aircraft, with the complete system less than 300 pounds
total when filled to capacity and not exceeding 2 ft. x 3 ft. x 5 ft.
(2 ft. being critical -- the width of the patient litter); (b) Oxygen
Generation -- minimum 33 (45 preferred) liters per minute of gaseous
oxygen at 50 psig for 16 hours; (c) Oxygen Distribution -- 3
distribution outlets required, capability to fill oxygen tanks,
desired; (d) Oxygen Quality > or equal to 93 percent purity; (e)
Emergency Operation -- must maintain oxygen delivery during power
termination for 2 hours minimum (4 hours desired); (f) Operating
Temperatures -- operate in temperatures of -24 to +140 degrees
Fahrenheit; (g) Electrical -- operate on worldwide hospital and
aircraft AC current, not to exceed 115-220 VAC, 50-400 HZ, 15 amps (10
amps maximum preferred), 5,000 watts (total), 28 VDC; and (h)
Certification -- Food and Drug Administration (FDA) certification of
conforming to FDA requirements for medical devices and U.S.
Pharmacopoeia (USP) requirements for hospital-grade oxygen. (2) Two
piece system that has the capability to produce, store and transfer
therapeutic oxygen to a "fly-away" component, which would be used to
deliver the therapeutic oxygen to meet patient requirements. Transfer
from production system to delivery system should be automated.
Equipment should have the following characteristics: (a) Human Factors:
Fly-away portion must be portable, compact, and compatible with use in
aircraft and weigh less than 300 pounds when filled to capacity, and
not exceeding 2 ft. x 3 ft. x 5 ft; Ground-based portion must be mobile
and easily transportable; (b) Oxygen Generation -- minimum 33 (45
preferred) liters per minute of gaseous oxygen at 50 psig for 16 hours;
(c) Oxygen Distribution: Flyaway unit must have minimum of three
distribution outlets; ground unit must fill one flyaway unit (three
simultaneously, desired) and have capability to fill high-pressure
oxygen tanks (desired); (d) Oxygen Quality:> or equal to 93.0
percent purity; (e) Emergency Operation- Fly-away unit must maintain
oxygen delivery during power termination for 2 hours minimum (4 hours
desired); (f) Operating Temperatures -- operate in temperatures of -24
to +140 degrees Fahrenheit, (g) Electrical -- operate on worldwide
hospital and aircraft AC current not to exceed 115-220 VAC, 50-400 HZ,
15 amps (10 amps preferred), 5,000 watts (total), 28 VDC; and (h)
Certification -- Food and Drug Administration (FDA) certification of
conforming to FDA requirements for medical devices and U.S.
Pharmacopoeia (USP) requirements for hospital-grade oxygen. Responses
for commercially available or developmental equipment should be
submitted. If commercially available items were procured by the Air
Force at a future date, minimal development funding is expected to be
required. Funding that would be available for equipment acquisition
would be for field testing to ensure reliability, maintainability,
ruggedness (vibration, drop, etc.), and environmental (heat, cold,
humidity, etc.), and compatibility to bring equipment into compliance
with those requirements. Submissions should identify how the equipment
is capable of meeting the above specifications. Responses should
include: (1) technical specifications that include all performance
capabilities and required interfaces, i.e., power, environmental, etc.;
(2) results of all testing that has been accomplished to date and any
planned future testing, along with a schedule to include
expected/actual performance/capability, reliability, maintainability,
and in-flight use; (3) current production rates of the equipment and
approximate delivery schedule; (4) logistics concepts for repairing and
maintaining the equipment; (5) any cost data available for the
equipment including unit, maintenance and operational life cycle,
either projected or actual; (6) manufacturing standards of thecompany;
and (7) current users of equipment. Capability statements, excluding
resumes, shall be submitted to 311 HSW/YAMA, 7909 Lindbergh Dr, Brooks
AFB, TX 78235-5232, within 30 days of publication of this notice. This
is a sources sought synopsis. This is not a request for proposal, and
in no way commits the Government to an award of contract. Reimbursement
of any cost regarding the preparation of proposals or bids will not be
made. TEHNICAL QUESTIONSMAY BE DIRECTED TO CAPT BILL SCHUM, 311
HSW/YAMA, (210)536-2367. All non-technical and contractual questions
should be addressed to 311 HSW/YAMA, Lt John Del Barrio, Contract
Manager (210) 536-2390, or Michael Nannery, Contracting Officer,
(210)536-4559. Posted 01/10/00 (W-SN414427). (0010) Loren Data Corp. http://www.ld.com (SYN# 0215 20000112\65-0004.SOL)
65 - Medical, Dental and Veterinary Equipment and Supplies Index Page
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