The Test Kit,cannabinoid Detection, cataloged under National Stock Number 6550-01-555-1563, 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 Microgenics Corporation Dba Microgenics Corp Div Clinical Diagnostics Division. Government technical data includes 2 specifications, 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. 2 items share a part number with this NSN in the catalog (possible match — not a government interchangeability claim). Current acquisition status: Active.
| Parameter | Value |
|---|---|
| NSN | 6550-01-555-1563 |
| Primary Part Number | 100091 |
| Item Name | Test Kit,cannabinoid Detection |
| FSC / FSG | 6550 / 65 — In Vitro Diagnostic Substances, Reagents, Test Kits and Sets |
| Manufacturer | Microgenics Corporation Dba Microgenics Corp Div Clinical Diagnostics Division |
| Status | ACTIVE |
| Test Media | URINE |
| Usage Design | IN-VITRO DIAGNOSTIC MEDICAL DEVICE INTENDED FOR QUALITATIVE AND SEMIQUANTITATIVE DETERMINATION OF CANNABINOIDS IN HUMAN URINE |
| 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 |
|---|---|
| 100091 PRIMARY | Microgenics Corporation Dba Microgenics Corp Div Clinical Diagnostics Division (USA) |
NSN 6550-01-555-1563 is a Test Kit,cannabinoid Detection, manufactured by Microgenics Corporation Dba Microgenics Corp Div Clinical Diagnostics Division, classified under FSC 6550, In Vitro Diagnostic Substances, Reagents, Test Kits and Sets. Status: active.
NSN 6550-01-555-1563 has 1 manufacturer part number on file: 100091 (Microgenics Corporation Dba Microgenics Corp Div Clinical Diagnostics Division).
2 possible matches (shared part number, not a government interchangeability claim): 4820-01-612-2499, 2510-01-694-5927. Verify interchangeability with system specifications before substitution.
Key specifications for 100091: Test Media: URINE; Part Name Assigned by Controlling Agency: CEDIA MUTLI LEVEL THC ASSAY; Usage Design: IN-VITRO DIAGNOSTIC MEDICAL DEVICE INTENDED FOR QUALITATIVE AND SEMIQUANTITATIVE DETERMINATION OF CANNABINOIDS IN HUMAN URINE. 2 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.