The Training Aid,catheter, cataloged under National Stock Number 6910-01-696-1913, is classified within Federal Supply Class 6910 (Training Aids) of the Training Aids and Devices group. The manufacturer of record is Prytime Medical Devices Inc. The record lists 2 manufacturer part numbers for this item, enabling identification through both NSN and commercial part number lookups. 2 additional reference documents (drawings, advisory and superseded references) are recorded in the U.S. Government catalog. Current acquisition status: Active.
| Parameter | Value |
|---|---|
| NSN | 6910-01-696-1913 |
| Primary Part Number | ER7232PLUS-R |
| Item Name | Training Aid,catheter |
| FSC / FSG | 6910 / 69 — Training Aids |
| Manufacturer | Prytime Medical Devices Inc |
| Status | ACTIVE |
| Acquisition Status | ACTIVE |
| DEMIL Code | DEMIL A — No Demilitarization Required |
| Hazard | No hazard code in the DLA record (HMIC N) |
| Criticality Code | X |
| Part Number | Manufacturer |
|---|---|
| ER7232PLUS-R | Red One Medical Devices Llc (USA) |
| ER7232PLUS-R PRIMARY | Prytime Medical Devices Inc (USA) |
| Reference | Meaning |
|---|---|
| 1598585 | 5/1 Secondary reference U.S. Government activity |
| 6515NCM217220 | 5/1 Secondary reference Defense Medical Standardization Board |
NSN 6910-01-696-1913 is a Training Aid,catheter, manufactured by Prytime Medical Devices Inc, classified under FSC 6910, Training Aids. Status: active.
NSN 6910-01-696-1913 has 2 manufacturer part numbers on file: ER7232PLUS-R (Red One Medical Devices Llc), ER7232PLUS-R (Prytime Medical Devices Inc).
Key specifications for ER7232PLUS-R: Special Features: ER-REBOA PLUS NON-STERILE TRAINING CATHETER; ER-REBOA PLUS CATHETER FOR USE IN EMERGENCY AND CRITICAL CARE, SUPPORTING RAPID AND IMMEDIATE HEMORRHAGE CONTROL. ER-REBOA PLUS CATHETER IS A PATENTED 7 FR COMPATIBLE BALLOON CATHETER FOR TEMPORARY OCCLUSION OF LARGE VESSELS FOR HEMORRHAGE CONTROL AND SUPPORTING ARTERIAL PRESSURE MONITORING. ONE PASS, GUIDEWIRE FREE DESIGN FACILITATES RAPID AND ACCURATE PLACEMENT. SOFT ATRAUMATIC P-TIP MINIMIZES THE RISK OF CATHETER MIGRATION INTO BRANCH VESSELS (PATENT PENDING). COMPLIANT BALLOON. LENGTH MARKS ALLOWING PHYSICIANS TO ADVANCE THE CATHETER TO THE DESIRED POSITION. BUILD-IN PRESSURE MONITORING LUMEN AND FLUOROSCOPY FREE INDICATION. FOR TRAINING ONLY; NOT FOR HUMAN USE.; Part Name Assigned by Controlling Agency: TRAINING AORTIC BALLOON CATHETER. 0 specifications are documented in the U.S. Government catalog.
No hazard code in the DLA record (HMIC N). Hazard information on this page is shown exactly as it appears in the DLA record.
U.S. Government catalog: edition PUBLOGDVD v12.0.0 (OCT 2026), edition date 2026-10-01, retrieved 2026-10-16.
U.S. Government catalog: edition PUBLOGDVD v12.0.0 (OCT 2026), edition date 2026-10-01, retrieved 2026-10-18.