The Control,fibrinogen, cataloged under National Stock Number 6550-01-237-3136, is classified within Federal Supply Class 6550 (In Vitro Diagnostic Substances, Reagents, Test Kits and Sets) of the Medical, Dental, and Veterinary Equipment group. 1 additional reference document (drawings, advisory and superseded references) is recorded in the U.S. Government catalog. Current acquisition status: Active.
| Parameter | Value |
|---|---|
| NSN | 6550-01-237-3136 |
| Item Name | Control,fibrinogen |
| FSC / FSG | 6550 / 65 — In Vitro Diagnostic Substances, Reagents, Test Kits and Sets |
| 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 |
| Reference | Meaning |
|---|---|
| B4233-22 | 3/9 Design control — primary reference Baxter Healthcare Corp Baxter Scientific Products Div Government Sales |
NSN 6550-01-237-3136 is a Control,fibrinogen, classified under FSC 6550, In Vitro Diagnostic Substances, Reagents, Test Kits and Sets. Status: active.
Key specifications for 6550-01-237-3136: Special Features: 1 ML VIAL; 10 VIAL; 10 VIALS PER PACKAGE; EACH VIAL CONTAINS LYOPHILIZED POWDER TO BE RECONSTITUTED WITH WATER TO 1 ML REQUIRES REFRIGERATION BETWEEN 2 AND 8 DEGREES CELSIUS; FOR USE IN ASSESSING THE ACCURACY OF LOW FIBRINOGEN. 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.