The Catheterization Kit,cardiovascul, cataloged under National Stock Number 6515-01-682-8835, 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 Teleflex Llc. The record lists 2 manufacturer part numbers for this item, enabling identification through both NSN and commercial part number lookups. 4 additional reference documents (drawings, advisory and superseded references) are recorded in the U.S. Government catalog. Current acquisition status: Active. Unit of issue: CS.
| Parameter | Value |
|---|---|
| NSN | 6515-01-682-8835 |
| Primary Part Number | AK-47702-P1A |
| Item Name | Catheterization Kit,cardiovascul |
| FSC / FSG | 6515 / 65 — Medical and Surgical Instruments, Equipment, and Supplies |
| Manufacturer | Teleflex Llc |
| 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 |
| Unit of Issue | CS |
| Part Number | Manufacturer |
|---|---|
| AK-47702-P1A PRIMARY | Teleflex Llc (USA) |
| ARWAK16702CDC | Medline Industries, Lp (USA) |
| Reference | Meaning |
|---|---|
| AK-16702-CDC | 5/9 Secondary reference Teleflex Medical Incorporated Dba Teleflex Medical Inc |
| 6515NCM195633 | 5/1 Secondary reference Defense Medical Standardization Board |
| 1557378 | 5/1 Secondary reference U.S. Government activity |
| AK-16702-CDC | 5/9 Secondary reference Teleflex Llc |
NSN 6515-01-682-8835 is a Catheterization Kit,cardiovascul, manufactured by Teleflex Llc, classified under FSC 6515, Medical and Surgical Instruments, Equipment, and Supplies. Status: active.
NSN 6515-01-682-8835 has 2 manufacturer part numbers on file: AK-47702-P1A (Teleflex Llc), ARWAK16702CDC (Medline Industries, Lp).
Key specifications for AK-47702-P1A: Special Features: CONTAINS ONE TWO-LUMEN INDWELLING CATHETER 7FR.X 20CM RADIOPAQUE POLYURETHANE WITH BLUE FLEXTIP, EXTENSION LINE CLAMPS; ONE SPRING-WIRE GUIDE 0.032" DIA. X 23-5/8"(STRAIGHT SOFT TIP ON ONE END"J" TIP ON OTHER); ONE INTRODUCER NEEDLE: 18GA. X 2-1/2" XTW; ONE INJECTION NEEDLE 25GA. X 1" AND 3 ML LUER-LOCK SYRINGE; ONE CATHETER 18GA. X 2-1/2" RADIOPAQUE OVER 20GA. RW INTRODUCER NEEDLE WITH 5ML LUER-SLIP SYRINGE; ONE INJECTION NEEDLE 22GA. X 1-1/2" AND 5ML LUER-SLIP SYRINGE; ONE LOCAL ANESTHETIC COMPONENTS; ONE TISSUE DILATOR; ONE 5ML 1% LIDOCAINE HCL SOLUTION; ONE 3 ML APPLICATOR 2% CHG AND 70% IPA CHLORAPREP ONE-STEP SOLUTION WITH HI-LITE ORANGE TINT; TWO DUST CAP NON-VENTED; ONE SECONDSITE ADJUSTABLE HUB FASTENER; ONE SECONDSITE ADJUSTABLE HUB CATHETER CLAAM; ONE SHARPSAWAY II LOCKING DISPOSAL CUP; ONE DRAPE 41" X 55" WITH 4" FENESTRATION; ONE SAFETY SCALPEL NO.11; TWO GAUZE PAD 2" X 2"; FIVE GAUZE PAD 4" X4"; ONE SUTURE 3-0 BRAIDED SILK WITH STRAIGHT NEEDLE. CM; Part Name Assigned by Controlling Agency: CENTRAL VENOUS CATHETER KIT TWO LUMEN STERILE. 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.