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No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00860017001274 1 FCP-09T Tactical Multi Bandage GAX Tourniquet, Nonpneumatic 1 The Emergency Bandage
2 00860017001281 B FCP-01 4" Military Bandage - US (Rev B) GAX Tourniquet, Nonpneumatic 1 The Emergency Bandage
3 00860017001267 1 FCP-T3 Tactical Trauma Treatment Bandage GAX Tourniquet, Nonpneumatic 1 The Emergency Bandage
4 00860017001250 1 FCP-06 Civilian Bandage 6" Width GAX Tourniquet, Nonpneumatic 1 The Emergency Bandage
5 00860017001243 1 FCP-03 Civilian Bandage 4" Width GAX Tourniquet, Nonpneumatic 1 The Emergency Bandage
6 00860017001236 1 FCP-02 Military Bandage 6" Width GAX Tourniquet, Nonpneumatic 1 The Emergency Bandage
7 00860017001229 1 FCP-01 Military Bandage 4" Width GAX Tourniquet, Nonpneumatic 1 The Emergency Bandage
8 00850026832006 1 NIO-P Pediatric NIO Intraosseous FMI Needle, Hypodermic, Single Lumen 2 NIO Next Generation IO
9 00850026832105 1 NIO FIXATION DRESSING KMK Device, Intravascular Catheter Securement 1 NIO NEXT GENERATION IO
10 00850026832037 1 NIO-A ADULT NIO INTRAOSSEOUS FMI Needle, Hypodermic, Single Lumen 2 NIO NEXT GENERATION IO
11 00850026832020 1 NIO-I INFANT NIO INTRAOSSEOUS FMI Needle, Hypodermic, Single Lumen 2 NIO NEXT GENERATION IO
12 00860017001298 1 THE EMERGENCY ELASTIC WRAP - 4" FQM Bandage, Elastic 1 THE EMERGENCY ELASTIC WRAP
13 00850026832075 1 WOUNDSTOP CARE 1 GAX Tourniquet, Nonpneumatic 1 THE EMERGENCY BANDAGE
14 00850026832068 1 WOUNDSTOP HOMECARE GAX Tourniquet, Nonpneumatic 1 THE EMERGENCY BANDAGE
15 00850026832051 1 FCP-10T TACTICAL CIVILIAN ABDOMINAL BANDAGE 8" WIDTH GAX Tourniquet, Nonpneumatic 1 THE EMERGENCY BANDAGE
16 00850026832044 1 FCP-09 MILITARY ABDOMINAL BANDAGE 8" WIDTH GAX Tourniquet, Nonpneumatic 1 THE EMERGENCY BANDAGE
17 00860017001205 1 Intraosseous Start Kit OJA Intravenous Extension Tubing Set GO IO
18 00850026832112 1 GO IO-F Intraosseous Start Kit w/ Fixation OJA Intravenous Extension Tubing Set 2 GO IO
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No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
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