Performance Matrix Attch 05.xlsx

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Amendment 03 Pending modification Tactical Combat Casualty Care
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H92222-10-R-0018
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Q A's 14 May 2010.pdf PDF
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Rqts Traceability Matrix

TACTICAL COMBAT CASUALTY CARE REQUIREMENTSMETHODS AND SCORINGSUSTAINMENT
E-1 MODULEE-2 MODULEE-3 MODULEM-1 MODULEM-2 MODULET-1 MODULET-2 MODULET-3 MODULET-4 MODULET-5 MODULET-6 MODULES-1 MODULES-2 MODULE
▼ SYSTEM ▼▼ REQUIREMENTS ▼
KITMODULEI.D. NUMBERSub - I.D. NUMBERSubSub - I.D. NUMBERDESCRIPTIONP-SPEC Ref. ParagraphATTRIBUTE CATEGORY▼ CRITERIA (quantifiable / measurable) ▼

Eugene Beal: Eugene Beal:

This explains how the item will be evaluated IAW the description of the requirement. A detailed 'scenario' or articulation of "We will evaluate this item by…." is needed.Maximum ScoreInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part numberInsert product nomenclature, model number, part number
CASEVACGENERAL1Employed by a trained SOF ATP/Corpsman4.1.1.1.Safety√√√√√10
2Medical items and protocols shall be within the ability of SOF ATPs to effectively employ in harsh environments4.1.1.1.1.Medical Protocols10
3Medical items and protocols shall be within the ability of SOF ATPs to effectively employ during limited visibility4.1.1.1.1.Medical Protocols10
4Medical items and protocols shall be within the ability of SOF ATPs to effectively employ; possibly even when wounded.4.1.1.1.1.Environment10
5Medical equipment and supplies shall be approved or cleared by the FDA and or the USSOCOM Surgeon General for use4.1.1.3.1.Regulatory Compliance10
6Equipment/supplies shall meet all applicable electrical safety standards and regulations to include but not limit to UL 544, and ANSI/AAMI HF-18 Electrical Safety Standards.4.1.1.3.2.Safety10
8All equipment/supply items required to perform the CASEVAC mission utilizing the latest technology, lightest weight, most compact design, integration of multiple capabilities, highest durability, and highest reliability (O).4.1.1.3.4.Equipment10
9CASEVAC kits shall be man-packable**4.1.1.4.1. 4.1.1.4.2.Lightweight10
10CASEVAC kits shall be man-portable**4.1.1.4.1. 4.1.1.4.3.Lightweight10
11Each kit shall be self-contained4.1.1.5.3.Modularity10
12Each kit shall be modularized4.1.1.5.3.Modularity10
13Each kit shall be able to be combined with/connected to other kits to the maximum extent practicable4.1.1.5.3.Modularity10
14Kit shall include all packaging necessary to transport/store all equipment/supply items in an organized manner4.1.1.5.1.Accessibility10
15Packaging shall include additional storage compartments to accommodate extra supplies or mission unique items4.1.1.5.2.Accessibility10
16Each man-packable kit shall be compact to the maximum extent practicable using snaps, zippers, hooks, straps, pouches, and pockets to streamline the design4.1.1.5.4.Equipment10
17Each man-portable kit shall consist of man-packable packaging4.1.1.5.5.Reliability10
18Each man-portable kit shall include ruggedized, air-worthy containers suitable to organize transport and protect the equipment/supplies stored within.4.1.1.5.5.Reliability10
19Each kit shall maintain usability and operate in the intended environment for a minimum of a two year life-cycle management period.4.1.1.6.1.Reliability10
20Each man-packable kit shall have reinforced stress points4.1.1.6.2.Reliability10
AAMean Time Between Failure (MTBF) for all medical electronic items:4.1.1.6.3.Reliability
Threshold:
A. The mean time between Operational Mission Failure will be at least 360 hours.
B. The operational availability will be .95 when operated over a 30-day period.
C. The mean time to repair will be 3 hours.
Objective:
A. The mean time between Operational Mission Failure will be at least 540 hours.
B. The operational availability will be .98 when operated over a 30-day period.
C. The mean time to repair will be 1 hour.
21Items contained in each kit shall be packaged so that they are no more than 1-zipper deep4.1.1.7.2.Accessibility10
22Each kit’s packaging shall include basic labels for each compartment4.1.1.7.3.Safety10
23Kit’s packaging shall allow the equipment and/or supplies to be accessible by SOF Operators wearing gloves4.1.1.7.4.Accessibility10
24Each kit shall have universal connectors, straps, and other attachments to safely and quickly secure the individual modules to SOF standard and non-standard mobility platforms4.1.1.8.1.Adaptability10
25Each kit shall meet all all requirements to be transported by aircraft IAW USAARL policies4.1.1.9.1.Air / Crash Worthy10
26Each kit shall meet all IAW USAARL policy requirements with respect to air and crash worthy packaging4.1.1.9.2.Air / Crash Worthy10
27Each kit shall meet SOF mission environmental requirements4.1.1.10.1.Environment10
28Each kit’s non-medical equipment/supplies and packaging shall have an operating temperature range of -25°F/-33°C to 120°F/49°C.4.1.1.10.2.Environment10
30Each kit’s medical equipment shall have an operating temperature range of 40°F/4°C to 120°F/49°C (T) -25°F/-33°C to 120°F/49°C (O).4.1.1.10.3.Environment10
32Each kit’s equipment/supplies and packaging shall have a storage/transport temperature range of -25°F/-33°C to 160°F/71°C.4.1.1.10.4.Environment10
34Each kit’s equipment/supplies and packaging shall be able to withstand shock and vibration expected during shipment or transport4.1.1.10.5.Air / Crash Worthy10
35Each kit’s packaging shall protect all equipment/supplies from moisture when prepared for transport4.1.1.10.6.Environment10
36Each kit’s packaging shall protect all equipment/supplies from high winds when prepared for transport4.1.1.10.6.Environment10
37Each kit’s packaging shall protect all equipment/supplies from dust and sand when prepared for transport4.1.1.10.6.Environment10
38Each kit’s packaging shall protect all equipment/supplies from other environmental hazards when prepared for transport4.1.1.10.6.Environment10
39Each kit’s electrical equipment shall be operated by batteries that are lightweight4.1.1.11.1.Power10
40Each kit’s electrical equipment shall be operated by batteries that are maintenance-free4.1.1.11.1.Power10
41Each kit’s electrical equipment shall be operated by batteries that are low-heat (O)4.1.1.11.1.Power10
42Each kit’s electrical equipment shall be operated by batteries that are extended-life4.1.1.11.1.Power10
43Each kit’s electrical equipment shall be operated by batteries that are rechargeable4.1.1.11.1.Power10
44The batteries shall be rechargeable by a 110/120VAC (T), 220/240VAC (T), 20VDC (O), 12VDC (O), non-standard voltage (O) power source.4.1.1.11.2.Power10
48The electrical equipment shall have the capability to operate off of the corresponding power source (O).4.1.1.11.3.Power10
49The electrical equipment shall utilize common batteries already in the Government system to the maximum extent practicable.4.1.1.11.3.Power10
50One common battery shall be used throughout all of the electronic equipment (O).4.1.1.11.3.Power10
52Each kit’s medical equipment shall be able to be maintained by Department of Defense medical maintenance personnel4.1.1.12.2.Maintenance10
53Each kit’s medical equipment shall be able to be repaired by Department of Defense medical maintenance personnel4.1.1.12.2.Maintenance10
54Each kit’s medical equipment shall be able to be calibrated by Department of Defense medical maintenance personnel4.1.1.12.2.Maintenance10
55Each kit shall have a sustainment selection criteria for the equipment and supplies based on the attribute such as availability,4.1.1.13.2.Sustainment10
56Each kit shall have a sustainment selection criteria for the equipment and supplies based on the attribute of shelf-life4.1.1.13.2.Sustainment10
57Each kit shall have a sustainment selection criteria for the equipment and supplies based on the attribute of lead-time4.1.1.13.2.Sustainment10
58Each kit shall have a sustainment selection criteria for the equipment and supplies based on the attribute of spare parts4.1.1.13.2.Sustainment10
59Each kit shall have a sustainment selection criteria for the equipment and supplies based on the attribute of supportability4.1.1.13.2.Sustainment10
60Each kit shall have a sustainment selection criteria for the equipment and supplies based on the attribute of warranty4.1.1.13.2.Sustainment10
61The CASEVAC Set’s equipment shall include two (2) each operator and service manuals per Kit/Module as required for reference.4.1.1.14.1.Documentation10
63Each CASEVAC Set module shall include a packing list detailing all items contained within and the item’s location made of paper (T) durable, readable fabric (O).4.1.1.14.2.Documentation10
KPPEach CASEVAC Set will come with appropriate training media, web based, Compact Disc (CD) or Digital Versatile Disc (DVD) to ensure adequate New Equipment Training and Refresher Training requirements are met with the least impact on operational schedules. Back up hard copy files will be made available on the TCCC web page.4.1.1.14.3.Training
EXTRACTIONOVERALL64All items incorporated into the Extraction Modules shall meet air worthy certification requirements4.1.2.1.1.Air / Crash Worthy10
65All items incorporated into the Extraction Modules shall meet crash worthy certification requirements4.1.2.1.1.Air / Crash Worthy10
66All items incorporated into the Extraction Modules shall meet National Fire Protection Agency (NFPA) standards.4.1.2.1.2.Safety10
67All items incorporated into the Extraction Modules shall meet United International Alpine Agency (UIAA) standards.4.1.2.1.2.Safety10
E - 168The E-1 Module shall be man-packable to be transported by one SOF Operator4.1.2.2.6.Lightweight10
69The E-1 Module shall have the capability to extricate casualties from all terrain to include water obstacles in transition to a rigid litter for ground/air evacuation.4.1.2.2.1.Environment10
69.1Terrain Types5
69.1.1Forest0.71
69.1.2Jungle0.71
69.1.3Rocky Desert0.71
69.1.4Sand Desert0.71
69.1.5Mountains0.71
69.1.6Water (Open water/ocean, littoral)0.71
69.1.7Water (River, Swamp, lake)0.71
70The E-1 Module shall have the capability to extricate casualties from all terrain to include water obstacles during day or night in transition to a rigid litter for ground/air evacuation.4.1.2.2.2.Environment10
70.1Day / light Capability5
70.2Night / darkness Capability5
71The E-1 Module shall have the capability to package a casualty with spinal injury4.1.2.2.3.Medical Protocols10
71.1Shall include straps capable of attaching to spinal immobilization board incorporating quick-disconnect single hand operation.4.1.2.2.3.1.5
71.2Shall incorporate cervical spine immobilization w/ tracheal access.4.1.2.2.3.2.5
72The E-1 Module shall have the capability to splint upper extremity fractures of casualties4.1.2.2.4.Medical Protocols10
73The E-1 Module shall have the capability to splint lower extremity fractures of casualties4.1.2.2.4.Medical Protocols10
74The E-1 Module shall have the capability to splint pelvic fractures of casualties4.1.2.2.4.Medical Protocols10
E - 275The E-2 Module shall be man-packable to be transported by one SOF Operator4.1.2.3.1.Lightweight10
76The E-2 Module shall have the capability to safely access and recover casualties from high angle terrain using rope and rigging equipment.4.1.2.3.2.Extreme Terrain10
77The E-2 Module shall have the capability to safely access and recover casualties from urban obstacles using rope and rigging equipment.4.1.2.3.2.Extreme Terrain10
78The E-2 Module shall have the capability for vertical hoist operations.4.1.2.3.4.Extreme Terrain10
78.1Static ropes shall be 150’ e-z bend with a TBD minimum strength3.33
78.2Rope bags shall be sized appropriately and will include rappelling gloves (as ordered) in small – Extra Extra Large (XXL) sizes, compatible ascenders, and locking gate carabineers.3.33
78.3Shall include a full body, adjustable rescue harness which is adjustable with lift capability.4.1.2.3.4.1.3.33
E - 379The E-3 Module shall be man-packable to be transported by one SOF Operator4.1.2.4.1.Lightweight10
80All items incorporated into the E-3 Module shall meet air worthy certification requirements4.1.2.1.1.Air / Crash Worthy10
81All items incorporated into the E-3 Module shall meet crash worthy certification requirements4.1.2.1.1.Air / Crash Worthy10
82The E-3 Module shall have the capability to pry and cut wreckage to facilitate rapid extrication4.1.2.4.2.Safety10
CommentShould be powered by either battery or diesel / JP8
83The E-3 Module shall have the capability to lift and move large objects, i.e. vehicles, wreckage, building debris, etc, high enough to remove casualties trapped underneath4.1.2.4.3.Safety10
83.1If pneumatic device is used, should be capable of using vehicle as primary air source
1
MOBILITYM - 184The M-1 Module shall be man-packable to be transported by one SOF Operator4.1.3.2.1.Lightweight10
84.1Backpack shall be available in multi-camouflage and/or earth tone patterns
84.2Backpack shall be capable of supporting provided litter
84.3Pack cover should provide weather and dust proof protection of casualty’s equipment
85All items incorporated into the M-1 Module shall meet air worthy certification requirements4.1.3.1.1.Air / Crash Worthy10
86All items incorporated into the M-1 Module shall meet air worthy certification requirements4.1.3.1.1.Air / Crash Worthy10
87All items incorporated in the M-1 Module shall meet SOF military specification standards for all terrain environments encountered as established by SOF prepotenciesNONEEnvironment10
88The M-1 Module shall have the capability to secure and safely transport a casualty on a rigid litter through all phases of TCCC to level III medical treatment4.1.3.2.2.Safety10
88.1Litter shall be collapsible to 20 inches in lengthA2.7.1.2.5
88.2Litter shall weigh less than 17 (T) 12 (O) poundsA2.7.2.2.5
88.3Litter shall have a capacity of 400 (T) 1200 (O) poundsA2.7.3.2.5
88.4Litter shall have two casualty straps that can withstand 5,500 pounds of forceA2.7.4.2.5
89The M-1 Module shall include a rigid litter that meets CBRNE Decontamination criteria4.1.3.2.3.Environment10
90The M-1 Module shall include a rigid litter that is hands-free (i.e. able to be moved using a strap, harness, etc. such that hands are free to use), self-contained and compatible with US/NATO medical evacuation transport equipment.4.1.3.2.3.Adaptability10
91The M-1 Module shall be compatible with MOLLE/PALS configurations4.1.3.2.4.Adaptability10
M - 292The M-2 Module shall be man-packable to be transported by one SOF Operator4.1.3.3.1.Lightweight10
93All items incorporated into the M-2 Module shall meet air worthy certification requirements4.1.3.1.1.Air / Crash Worthy10
94All items incorporated into the M-2 Module shall meet crash worthy certification requirements4.1.3.1.1.Air / Crash Worthy10
95The M-2 Module shall transport the M-1 Module in a modular format4.1.3.3.2.Modularity10
96The M-2 Module shall have the capability to attach the rigid litter from the M-1 Module to current SOF ground/air mobility or ad hoc platforms4.1.3.3.3.Adaptability10
97The M-2 Module shall have the capability to provide day/night landing zone marking4.1.3.3.4.Safety10
98The M-2 Module shall have the capability to mark basic triage categories on casualties4.1.3.3.5.Medical Protocols10
98.1Immediate, Urgent, Delayed, Expectant
99The M-2 Module shall have the capability to carry additional initial TCCC medical supplies4.1.3.3.6.Adaptability10
99.1Reflective warming blankets shall incorporate warming cells0.83
99.2Nitrile gloves shall be provided at a minimum of two pair per size per kit and be of a color to best identify bleeding of the casualty0.83
9.3Headlamps shall provide for blood identification, utilize a common battery and be capable of multiple color lighting (LED, IR, Green, White & Red)0.83
99.4Shall have a blunt tipped seatbelt cutting tool capable of window breakage [straight blade blunt tip knife].4.1.3.3.6.1.0.83
99.5Shall include a Bandage, 6" Emergency, w/ Mobile Pad4.1.3.3.6.2.0.83
99.6Shall include Unit, catheter-Needle, IV 14gauge x 3.25"4.1.3.3.6.2.0.83
99.7Shall include Airway, Nasopharyngeal, 28 French4.1.3.3.6.2.0.83
9.8Shall include Pack, Surgical Lubricant4.1.3.3.6.2.0.83
99.9Shall include Dressing, Hemostatic Gauze, Combat4.1.3.3.6.2.0.83
99.10Shall include Bandage, Occlusive Chest Wound4.1.3.3.6.2.0.83
99.11Trauma shears shall have blunt tips to ensure that patients are not further injured4.1.3.3.6.2.0.83
99.12Shall include a tourniquet which is small and lightweight with one-handed operation4.1.3.3.6.3.0.83
100The M-2 Module shall be compatible with MOLLE/PALS configurations4.1.3.3.7.Adaptability10
TRANSPORTATIONT - 1101The T-1 module shall incorporate all accessories and supplies necessary to operate and charge the associated pieces of medical equipment4.1.4.1.2.Power10
102All medical equipment contained within the T-1 module shall meet air worthy requirements.4.1.4.1.4.Air / Crash Worthy10
103All medical equipment contained within the T-1 module shall meet crash worthy requirements.4.1.4.1.4.Air / Crash Worthy10
104The T-1 module shall be capable of being man-portable when combined with other Transport modules4.1.4.2.2.Lightweight10
105The T-1 module itself shall be capable of being man-packable4.1.4.2.1.Lightweight10
106The T-1 Module shall have the capability to monitor casualty vital signs4.1.4.2.3.Medical Protocols10
106.1Blood Pressure (T)4.1.4.2.3.0.9
106.2Oxygen Saturation (T)4.1.4.2.3.0.9
106.3Cardiac Output (T)4.1.4.2.3.0.9
106.4Heart Rate (T)4.1.4.2.3.0.9
106.5Temperature (O)4.1.4.2.3.0.9
106.6Carbon Dioxide Levels (O)4.1.4.2.3.0.9
106.7The device (s) will have a readable screen under any light or light sensitive condition4.1.4.2.3.0.9
106.8The device (s) will have the ability to manually cancel audio-visual alarms.4.1.4.2.3.0.9
106.9The device (s) shall include a Thermometer- Digital, Clinical.4.1.4.2.3.0.9
106.10Monitor shall have a casing either internal or external that protects the monitor from damage during operation4.1.4.2.3.0.9
106.11Monitor shall be water resistant. (O)4.1.4.2.3.0.9
T - 2107The T-2 module shall incorporate all accessories and supplies necessary to operate and charge the associated pieces of medical equipment4.1.4.3.1..Power10
108All medical equipment contained within the T-2 module shall meet air worthy requirements.4.1.4.1.4.Air / Crash Worthy10
109All medical equipment contained within the T-2 module shall meet crash worthy requirements.4.1.4.1.4.Air / Crash Worthy10
110The T-2 module shall be capable of being man-portable when combined with other Transport modules4.1.4.3.3.Modularity10
111The T-2 module itself shall be capable of being man-packable4.1.4.3.2.Lightweight10
112The T-2 Module shall have the capability to provide casualty electric cardiac therapy4.1.4.3.4.Medical Protocols10
112.1Defibrillator shall be an automated external defibrillator (AED)4.1.4.3.4.3.33
112.2Defibrillator shall perform cardiac output monitoring with visual display4.1.4.3.4.3.33
112.3Defibrillator shall have an integrated external noninvasive pacemaker (O)3.33
112.3The device (s) will have a readable screen under any light or light sensitive condition4.1.4.3.4.
112.4The device (s) will have the ability to manually cancel audio-visual alarms4.1.4.3.4.
T - 3113The T-3 module shall incorporate all accessories and supplies necessary to operate and charge the associated pieces of medical equipment4.1.4.4.1.Medical Protocols10
114All medical equipment contained within the T-3 module shall meet air worthy requirements.4.1.4.1.4.Air / Crash Worthy10
115All medical equipment contained within the T-3 module shall meet crash worthy requirements.4.1.4.1.4.Air / Crash Worthy10
116The T-3 module shall be capable of being man-portable when combined with other Transport modules4.1.4.4.2.Lightweight10
117The T-3 module itself shall be capable of being man-packable4.1.4.4.3.Lightweight10
118The T-3 Module shall have the capability to provide casualty mechanical ventilation4.1.4.4.5.Medical Protocols10
118.1to be used with the oxygen generation capability4.1.4.4.5.2.5
118.2This module shall include Advanced Airway Management capability4.1.4.4.5.2.5
118.3Shall have audible and visual alarms that can be silenced/adjusted for all critical parameters.4.1.4.4.5.2.5
119The T-3 Module shall have the capability to generate a fraction of inspired oxygen (FiO2) of 50% without use of a pressurized cylinder.4.1.4.4.4.Medical Protocols10
T - 4120The T-4 module shall incorporate all accessories and supplies necessary to operate and charge the associated pieces of medical equipment4.1.4.5.1.Power10
121All medical equipment contained within the T-4 module shall meet air worthy requirements.4.1.4.1.4.Air / Crash Worthy10
122All medical equipment contained within the T-4 module shall meet crash worthy requirements.4.1.4.1.4.Air / Crash Worthy10
123The T-4 module shall be capable of being man-portable when combined with other Transport modules4.1.4.5.2.Modularity10
124The T-4 module itself shall be capable of being man-packable4.1.4.5.3.Lightweight10
125The T-4 Module shall have the capability to monitor casualty bodily fluid input and output.4.1.4.5.7.Medical Protocols10
126The T-4 Module shall have the capability to store and transport standard blood storage bags.4.1.4.5.4.Adaptability10
127The T-4 Module shall have the capability to provide controlled casualty fluid resuscitation administered intravenously4.1.4.5.6.Medical Protocols10
127.1IV Pump shall be no larger than 65 in3 with any one dimension not to exceed 6 in.4.1.4.5.6.
128The T-4 Module shall have the capability to warm blood to 32° C (T) 38° C (O) for casualty transfusions.4.1.4.5.5.Medical Protocols10
128.1Fluid warming device shall be an inline fluid warmer2.5
128.2Fluid warming device shall warm the fluid to 100°F/38°C2.5
128.3Fluid warming device shall have an adjustable flow rate of 2-150 mL/min2.5
128.4Fluid warming device shall have an integrated infusion pump (O)2.5
T - 5129All medical equipment contained within the T-5 module shall meet air worthy requirements.4.1.4.1.4.Air / Crash Worthy10
130All medical equipment contained within the T-5 module shall meet crash worthy requirements.4.1.4.1.4.Air / Crash Worthy10
131The T-5 module shall be capable of being man-portable when combined with other Transport modules4.1.4.6.1.Lightweight10
132The T-5 module itself shall be capable of being man-packable4.1.4.6.2.Lightweight10
133The T-5 Module shall have the capability to warm casualties with decreased bodily temperature using a full-body wrap with hood and heatpacs4.1.4.6.3.Medical Protocols10
134The T-5 module shall be capable of warming casualties in cold temperatures4.1.4.6.4.Medical Protocols10
T - 6135All medical equipment contained within the T-6 module shall meet air worthy requirements.4.1.4.1.4.Air / Crash Worthy10
136All medical equipment contained within the T-6 module shall meet crash worthy requirements.4.1.4.1.4.Air / Crash Worthy10
137The T-6 module shall be capable of being man-portable when combined with other Transport modules4.1.4.7.1.Lightweight10
138The T-6 module itself shall be capable of being man-packable4.1.4.7.2.Lightweight10
139The T-6 Module shall have the capability to mount the medical equipment contained in modules 1-5 within the Transport Modules to the rigid litter specified in the Mobility Module4.1.4.7.3.Modularity10
139.1Shall mount anywhere on a standard NATO litter and be capable of holding portable medical equipment, to include:
139.1.1Ventilator1.66
139.1.2Suction1.66
139.1.3Monitor1.66
139.1.4Infusion pump1.66
139.1.5Power supply1.66
139.1.6Steel and carbon-fiber oxygen cylinders1.66
SUSTAINMENTS - 1140All medical equipment contained within the S-1 module shall meet air worthy requirements.4.1.5.1.2.Air / Crash Worthy10
141All medical equipment contained within the S-1 module shall meet crash worthy requirements.4.1.5.1.2.Air / Crash Worthy10
142The S-1 Module shall be man-packable to be transported by one SOF Operator4.1.5.2.1.Lightweight10
143The S-1 Module shall have the capability to provide and sustain the control of life-threatening bleeding for up to four hours4.1.5.2.2.Power10
143.1Shall include a pressure dressing with built in tension bar
144The S-1 Module shall have the capability to provide and sustain the treatment and prevention of shock for up to four hours4.1.5.2.3.Medical Protocols10
145The S-1 Module shall have the capability to provide and sustain the protection of wounds to include burns from contamination, infection or further injury for up to four hours4.1.5.2.4.Medical Protocols10
146The S-1 Module shall have the capability to provide and sustain pain management without adverse affects for up to four hours4.1.5.2.5.Medical Protocols10
147The S-1 Module shall have the capability to provide and sustain the control of vomiting for up to four hours4.1.5.2.6.Medical Protocols10
148The S-1 Module shall have the capability to provide additional TCCC Operator and Medic Kits supplies for additional Operators4.1.5.2.8.Modularity10
S - 2149All medical equipment contained within the S-2 module shall meet air worthy requirements.4.1.5.1.2.Air / Crash Worthy10
150All medical equipment contained within the S-2 module shall meet crash worthy requirements.4.1.5.1.2.Air / Crash Worthy10
151The S-2 Module shall be man-packable to be transported by one SOF Operator4.1.5.3.1.Lightweight10
152The S-2 Module shall have the capability to provide advanced airway care up to and including surgical airway procedures4.1.5.3.2.Medical Protocols10
152.1Suction kits shall be manual and disposable.
152.2Combi-tube, Trachial, Airway shall be of sizes 4, 5 & 6 and be non-latex.
152.3Nitrile gloves shall be provided in XL size and be of a color (green) to best identify bleeding of the casualty.
152.4Laryngoscope blades will be both metal/durable and disposable to include both Miller #3 and Macintosh #3 types and the handles will be fiber optic utilizing AA batteries. . A minimum of 48 AA batteries must be supplied.
152.5Forceps shall be angled to guide a tracheal tube into the larynx or a nasogastric tube into the esophagus under direct vision. They shall also be capable of placing pharyngeal packs and removing foreign bodies.
153The S-2 Module shall have the capability to provide casualty mechanical ventilation (T) to be used with an oxygen generation capability giving a fraction of inspired oxygen (FiO2) of 50% (O).4.1.5.3.3.Medical Protocols10

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