The Test Kit,imuclone, cataloged under National Stock Number 6550-01-574-4440, 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 American Diagnostica, Inc.. Government technical data includes 1 specification, 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 | 6550-01-574-4440 |
| Primary Part Number | 602 |
| Item Name | Test Kit,imuclone |
| FSC / FSG | 6550 / 65 — In Vitro Diagnostic Substances, Reagents, Test Kits and Sets |
| Manufacturer | American Diagnostica, Inc. |
| Status | ACTIVE |
| General Characteristics Item Description | MEASURES D-DIMER, CROSS LINKED FIBRIN DEGRADATION PRODUCT (XL-FDP), IN HUMAN PLASMA; ELEVATED XL-FDP LEVELS INDICATE REACTIVE FIBRINOLYSIS AND ARE FOUND IN A NUMBER OF ARTERIAL AND VENOUS OCCLUSIVE DISEASE STATES, INCLUDING ACUTE MYOCARDIAL INFARCTION (MI), DEEP VEIN THROMBOSIS (DVT), PULMONARY EMBOLISN (PE) AND DISSEMINATED INTRAVASCULAR COAGULATION (DIC); ELEVATED XL-FDP HAS ALSO BEEN REPORTED IN SURGERY, TRAUMA, SICKLE CELL DISEASE, LIVER DISEASE, SEVERE INFECTION, SEPSIS, INFLAMMATION, MALIGNANCY AND COMPLICATIONS DURING PREGNANCY; DETERMINATIONS OF XL-FDP LEVELS HAVE BEEN USED TO MONITOR THE COURSE AND RESPONSE TO THROMBOLYTIC THERAPY |
| Acquisition Status | ACTIVE |
| DEMIL Code | DEMIL A — No Demilitarization Required |
| Hazard | Possible hazard — SDS may be required (DLA HMIC P) |
| Criticality Code | X |
| Part Number | Manufacturer |
|---|---|
| 602 PRIMARY | American Diagnostica, Inc. (USA) |
NSN 6550-01-574-4440 is a Test Kit,imuclone, manufactured by American Diagnostica, Inc., classified under FSC 6550, In Vitro Diagnostic Substances, Reagents, Test Kits and Sets. Status: active.
NSN 6550-01-574-4440 has 1 manufacturer part number on file: 602 (American Diagnostica, Inc.).
Key specifications for 602: General Characteristics Item Description: MEASURES D-DIMER, CROSS LINKED FIBRIN DEGRADATION PRODUCT (XL-FDP), IN HUMAN PLASMA; ELEVATED XL-FDP LEVELS INDICATE REACTIVE FIBRINOLYSIS AND ARE FOUND IN A NUMBER OF ARTERIAL AND VENOUS OCCLUSIVE DISEASE STATES, INCLUDING ACUTE MYOCARDIAL INFARCTION (MI), DEEP VEIN THROMBOSIS (DVT), PULMONARY EMBOLISN (PE) AND DISSEMINATED INTRAVASCULAR COAGULATION (DIC); ELEVATED XL-FDP HAS ALSO BEEN REPORTED IN SURGERY, TRAUMA, SICKLE CELL DISEASE, LIVER DISEASE, SEVERE INFECTION, SEPSIS, INFLAMMATION, MALIGNANCY AND COMPLICATIONS DURING PREGNANCY; DETERMINATIONS OF XL-FDP LEVELS HAVE BEEN USED TO MONITOR THE COURSE AND RESPONSE TO THROMBOLYTIC THERAPY; Special Features: SPECIFICATIONS: SAMPLES: CITRATE OR EDTA COLLECTED PLASMA;PRECISION: INTRA-ASSAY LESS THAN 10 PERCENT; SAMPLE PREPARATION: 1:50 DILUTION;LOWER LIMIT OF DETECTION: 2 NG/ML; ASSAY TIME: 2.25 HOURS; STANDARD RANGE: 0-200 NG/ML;KIT COMPONENTS: 96-WELL ANTIBODY COATED PLATE,SAMPLE DILUENT,D-DIMER CALIBRATOR,HIGH CONTROL PLASMA,LOW CONTROL PLASMA,DETECTION ANTIBODY,DETECTION ANTIBODY DILUENT,SUBSTRATE,WASH BUFFER,STOP SOLUTION; Part Name Assigned by Controlling Agency: TEST KIT, IMUCLONE D-DIM2179 ER. 1 specification is 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.