The Catheter,arterial Radial, cataloged under National Stock Number 6515-01-695-9754, is classified within Federal Supply Class 6515 (Medical and Surgical Instruments, Equipment, and Supplies) of the Medical, Dental, and Veterinary Equipment group. The manufacturer of record is Prytime Medical Devices Inc. Government technical data includes 1 specification, cited from the U.S. Government catalog. 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through both NSN and commercial part number lookups. 2 additional reference documents (drawings, advisory and superseded references) are recorded in the U.S. Government catalog.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. Unit of issue: EA.
| Parameter | Value |
|---|---|
| NSN | 6515-01-695-9754 |
| Primary Part Number | ER7232PLUS |
| Item Name | Catheter,arterial Radial |
| FSC / FSG | 6515 / 65 — Medical and Surgical Instruments, Equipment, and Supplies |
| Manufacturer | Prytime Medical Devices Inc |
| Status | ACTIVE |
| Supplementary Features | LANDING ZONE MARKERS; DOCUMENTATION TAG; GUIDEWIERE COMPATIBLE. |
| Acquisition Status | ACTIVE |
| DEMIL Code | DEMIL A — No Demilitarization Required |
| Hazard | No hazard code in the DLA record (HMIC N) |
| Criticality Code | X |
| Unit of Issue | EA |
| Part Number | Manufacturer |
|---|---|
| ER7232PLUS PRIMARY | Prytime Medical Devices Inc (USA) |
| ER7232PLUS | Red One Medical Devices Llc (USA) |
| Reference | Meaning |
|---|---|
| 6515NCM217219 | 5/1 Secondary reference Defense Medical Standardization Board |
| 1598580 | 5/1 Secondary reference U.S. Government activity |
NSN 6515-01-695-9754 is a Catheter,arterial Radial, manufactured by Prytime Medical Devices Inc, classified under FSC 6515, Medical and Surgical Instruments, Equipment, and Supplies. Status: active.
NSN 6515-01-695-9754 has 2 manufacturer part numbers on file: ER7232PLUS (Prytime Medical Devices Inc), ER7232PLUS (Red One Medical Devices Llc).
Key specifications for ER7232PLUS: Supplementary Features: LANDING ZONE MARKERS; DOCUMENTATION TAG; GUIDEWIERE COMPATIBLE.; Special Features: THE ER-REBOA PLUS CATHETER IS INTENDED FOR TEMPORARY OCCLUSION OF LARGE VESSELS AND BLOOD PRESSURE MONITORING INCLUDING PATIENTS REQUIRING EMERGENCY CONTROL OF HEMORRAHAGE. A PATENTED 7 FR COMPATIBLE BALLOON CATHETER FOR TEMPORARY OCCLUSION OF LARGE VESSELS FOR HEMORRHAGE CONTROL WHILE SUPPORTING ARTERIAL PRESSURE MONITORING. THIS PATENTED DESIGN ENABLES SAFE AND EFFECTIVE PLACEMENT. 7 FR SHEATH COMPATIBILITY WHICH REDUCES THE NEED FOR SURGICAL REPAIR AT THE ACCESS SITE. ONE PASS, GUIDEWIRE FREE DESIGN FACILITATES RAPID AND ACCURATE PLACEMENT. SOFT ATRAUMATIC P-TIP PREVENTING 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. NEW FEATURES: PEEL AWAY SHEATH IS PACKAGED OVER THE BALLOON TO REDUCE PREP TIME; DUAL-SIDED LENGTH MARKER ARE NOW ON BOTH SIDE;; Part Name Assigned by Controlling Agency: AORTIC BALLOON CATHETER. 1 specification is 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.