The Guide Wire,cardiovascular Cathet, cataloged under National Stock Number 6515-01-573-0608, 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 Ev3 Inc. Dba Covidien. Government technical data includes 2 specifications, cited from the U.S. Government catalog. The record lists 1 manufacturer part number for this item, enabling identification through both NSN and commercial part number lookups. Current acquisition status: Active.
| Parameter | Value |
|---|---|
| NSN | 6515-01-573-0608 |
| Primary Part Number | 103-0602-300 |
| Item Name | Guide Wire,cardiovascular Cathet |
| FSC / FSG | 6515 / 65 — Medical and Surgical Instruments, Equipment, and Supplies |
| Manufacturer | Ev3 Inc. Dba Covidien |
| Status | ACTIVE |
| Overall Diameter | 0.014 INCHES NOMINAL IN |
| Material | STEEL CORROSION RESISTING OVERALL |
| 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 |
|---|---|
| 103-0602-300 PRIMARY | Ev3 Inc. Dba Covidien (USA) |
NSN 6515-01-573-0608 is a Guide Wire,cardiovascular Cathet, manufactured by Ev3 Inc. Dba Covidien, classified under FSC 6515, Medical and Surgical Instruments, Equipment, and Supplies. Status: active.
NSN 6515-01-573-0608 has 1 manufacturer part number on file: 103-0602-300 (Ev3 Inc. Dba Covidien).
Key specifications for 103-0602-300: Overall Diameter: 0.014 INCHES NOMINAL IN; Overall Length: 300.0 CENTIMETERS NOMINAL CM; Special Features: WITH A RADIOPAQUE PLATINUM DISTAL COIL; HYDROPHILICALLY COATED ON THE DISTAL PORTION; PROXIMAL PORTION COATED WITH POLYTETRAFLUOROETHYLENE; INCLUDED WITH THE STERILE POUCH IS A TORQUE DEVICE TO ASSIST GUIDEWIRE MANIPULATION AND GUIDEWIRE INTRODUCER; FOR GENERAL INTRAVASCULAR USE TO AID IN THE SELECTIVE PLACEMENT OF CATHETERS IN THE PERIPHERAL, VISCERAL AND CEREBRAL VASCULATURE DURING DIAGNOSTIC AND/OR THERAPEUTIC PROCEDURES; Part Name Assigned by Controlling Agency: X-CELERATOR HYDROPHILIC EXCHANGE GUIDEWIRE. 2 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.