The Test Kit,cutaneous Leishmaniasis, cataloged under National Stock Number 6550-01-633-9195, 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 Inbios International Inc. 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through both NSN and commercial part number lookups. 2 additional reference documents (drawings, advisory and superseded references) are recorded in the U.S. Government catalog.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: KT.
| Parameter | Value |
|---|---|
| NSN | 6550-01-633-9195 |
| Primary Part Number | CL025 |
| Item Name | Test Kit,cutaneous Leishmaniasis |
| FSC / FSG | 6550 / 65 — In Vitro Diagnostic Substances, Reagents, Test Kits and Sets |
| Manufacturer | Inbios International Inc |
| 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 | KT |
| Part Number | Manufacturer |
|---|---|
| CL025 PRIMARY | Inbios International Inc (USA) |
| Reference | Meaning |
|---|---|
| 6550NCM141607 | 5/1 Secondary reference Defense Medical Standardization Board |
| 1270069 | 5/1 Secondary reference U.S. Government activity |
NSN 6550-01-633-9195 is a Test Kit,cutaneous Leishmaniasis, manufactured by Inbios International Inc, classified under FSC 6550, In Vitro Diagnostic Substances, Reagents, Test Kits and Sets. Status: active.
NSN 6550-01-633-9195 has 1 manufacturer part number on file: CL025 (Inbios International Inc).
Key specifications for CL025: Special Features: CL DETECT RAPID TEST FOR CUTANEOUS LEISHMANIASIS; FDA-CLEARED, HAND-HELD, QUALITATIVE, IN VITRO IMMUNOCHROMATOGRAPHIC ASSAY FOR THE RAPID DETECTION OF LEISHMANIA SPECIES ANTIGEN IN ULCERATIVE SKIN LESIONS; INTENDED FOR USE WITH SAMPLES TAKEN WITH A DENTAL BROACH FROM ULCERATIVE SKIN LESIONS LESS THAN FOUR MONTHS OLD OBTAINED FROM PATIENTS WITH SUSPECTED CUTANEOUS LEISHMANIASIS (CL); FOR 25 TESTS; STORED AT ROOM TEMPERATURE (20-30 DEGREES CELSIUS); Part Name Assigned by Controlling Agency: IN VITRO IMMUNOCHROMATOGRAPHIC ASSAY FOR RAPID DETECTION OF LEISHMANIA. 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.