The Test Kit,fecal Rapid, cataloged under National Stock Number 6550-01-671-9301, 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 Rapid Dx North America Llc Dba Alere North America Llc. The record lists 2 manufacturer part numbers 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through both NSN and commercial part number lookups. 2 additional reference documents (drawings, advisory and superseded references) are recorded in the U.S. Government catalog.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: PG.
| Parameter | Value |
|---|---|
| NSN | 6550-01-671-9301 |
| Primary Part Number | T30407 |
| Item Name | Test Kit,fecal Rapid |
| FSC / FSG | 6550 / 65 — In Vitro Diagnostic Substances, Reagents, Test Kits and Sets |
| Manufacturer | Abbott Rapid Dx North America Llc Dba Alere North America Llc |
| 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 | PG |
| Part Number | Manufacturer |
|---|---|
| 23-046-789 | Fisher Scientific Co (USA) |
| T30407 PRIMARY | Abbott Rapid Dx North America Llc Dba Alere North America Llc (USA) |
| Reference | Meaning |
|---|---|
| 6550NCM184219 | 5/1 Secondary reference Defense Medical Standardization Board |
| 1511927 | 5/1 Secondary reference U.S. Government activity |
NSN 6550-01-671-9301 is a Test Kit,fecal Rapid, manufactured by Abbott Rapid Dx North America Llc Dba Alere North America Llc, classified under FSC 6550, In Vitro Diagnostic Substances, Reagents, Test Kits and Sets. Status: active.
NSN 6550-01-671-9301 has 2 manufacturer part numbers on file: 23-046-789 (Fisher Scientific Co), T30407 (Abbott Rapid Dx North America Llc Dba Alere North America Llc).
Key specifications for T30407: Special Features: A RAPID MEMBRANE EIA TEST FOR DETECTION OF GIARIA LAMBLIA AND CRYPTOSPORIDIUM PAVRUM IN STOOL. THE GIARDIA/CRYPTOSPORIDIUM CHEK; TEST IS AN ENZYME IMMUNOASSAY (ELISA) USED TO DETECT GIARDIA LAMBLIA AND CRYPTOSPORIDIUM IN FECAL SPECIMENS; IT IS INDICATED FOR USE AS AN AID IN THE DIAGNOSIS OF PATIENTS WITH DIARRHEA SUSPECTED OF GIARDIA AND/OR CRYTOSPORIDIUM GASTROINTESINTAL INFECTIONS; RESULTS IN 30 MINUTES WITHOUT INSTRUMENTATION; CLIA: MODERATE COMPLEXITY. GIARDIA SENSITIVITY 98.9 PERCENT, SPECIFICITY 100 PERCENT. CRYPTO SENSITIVITY 100 PERCENT, SPECIFICITY 99.8 PERCENT. 25 TESTS.; Part Name Assigned by Controlling Agency: FECAL PARASITE TEST KIT; RAPID GIARDIA, CRYPTOSPORIDIUM, 25'S. 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.