The Cartridge,coagulation Test, cataloged under National Stock Number 6550-01-718-7206, is classified within Federal Supply Class 6550 (In Vitro Diagnostic Substances, Reagents, Test Kits and Sets) of the Medical, Dental, and Veterinary Equipment group. The manufacturer of record is Abbott Laboratories Inc. Div Abbott Point of Care. The record lists 1 manufacturer part number 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through both NSN and commercial part number lookups. 2 additional reference documents (drawings, advisory and superseded references) are recorded in the U.S. Government catalog.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: BX.
| Parameter | Value |
|---|---|
| NSN | 6550-01-718-7206 |
| Primary Part Number | 03P89-50 |
| Item Name | Cartridge,coagulation Test |
| FSC / FSG | 6550 / 65 — In Vitro Diagnostic Substances, Reagents, Test Kits and Sets |
| Manufacturer | Abbott Laboratories Inc. Div Abbott Point of Care |
| Status | ACTIVE |
| Acquisition Status | ACTIVE |
| DEMIL Code | DEMIL A — No Demilitarization Required |
| Hazard | Possible hazard — SDS may be required (DLA HMIC P) |
| Criticality Code | X |
| Unit of Issue | BX |
| Part Number | Manufacturer |
|---|---|
| 03P89-50 PRIMARY | Abbott Laboratories Inc. Div Abbott Point of Care (USA) |
| Reference | Meaning |
|---|---|
| 6550NCM249660 | 5/1 Secondary reference Defense Medical Standardization Board |
| 1666088 | 5/1 Secondary reference U.S. Government activity |
NSN 6550-01-718-7206 is a Cartridge,coagulation Test, manufactured by Abbott Laboratories Inc. Div Abbott Point of Care, classified under FSC 6550, In Vitro Diagnostic Substances, Reagents, Test Kits and Sets. Status: active.
NSN 6550-01-718-7206 has 1 manufacturer part number on file: 03P89-50 (Abbott Laboratories Inc. Div Abbott Point of Care).
Key specifications for 03P89-50: Special Features: THE I-STAT PT PLUS CARTRIDGE IS INTENDED FOR USE IN THE IN VITRO QUANTITATIVE MEASUREMENT OF THE CLOT TIME OF THE EXTRINSIC COAGULATION PATHWAY WHEN WHEN ACTIVATED BY THROMBOPLASTIN IN NON-ANTICOAGULATED WHOLE BLOOD (VENOUS OR CAPILLARY), USING THE I-STAT 1 SYSTEM. MEASUREMENTS OF PROTHROMBIN TIME ARE USED TO AID IN THE MONITORING OF PATIENTS RECEIVING ANTICOAGULANT THERAPY WITH COUMARIN DERIVATIVES. THE I-STAT PT PLUS PT TEST RESULT IS REPORTED IN SECONDS AND AS AN INR. THE TEST IS INTENDED FOR POINT OF CARE USE AND IS FOR PRESCRIPTION USE ONLY.; Part Name Assigned by Controlling Agency: I-STAT PT PLUS CARTRIDGE 25EA. 0 specifications are documented in the U.S. Government catalog.
Possible hazard — SDS may be required (DLA HMIC P). 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.