The Test Kit,human Chorionic Gonadot, cataloged under National Stock Number 6550-01-607-9206, 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 Quidel Corp. Government technical data includes 4 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through both NSN and commercial part number lookups. 2 additional reference documents (drawings, advisory and superseded references) are recorded in the U.S. Government catalog.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 | 6550-01-607-9206 |
| Primary Part Number | 20110 |
| Item Name | Test Kit,human Chorionic Gonadot |
| FSC / FSG | 6550 / 65 — In Vitro Diagnostic Substances, Reagents, Test Kits and Sets |
| Manufacturer | Quidel Corp |
| Status | ACTIVE |
| Test Media | SERUM OR URINE |
| Test Capability Quantity | 50 |
| Usage Design | USES A MONOCLONAL ANTIBODY SPECIFIC TO THE BETA SUBUNIT OF HUMAN CHORIONIC GONADOTROPIN (HCG) TO ACCURATELY DETECT HCG |
| Component Breakdown Within Each Test Kit | (50) INDIVIDUALLY WRAPPED TEST CASETTES, (50) DISPOSABLE PIPETTES, (1) PACKAGE INSERT, (1) PROCEDURE CARD |
| 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 |
|---|---|
| 20110 PRIMARY | Quidel Corp (USA) |
| Reference | Meaning |
|---|---|
| 6550NCM127929 | 5/1 Secondary reference Defense Medical Standardization Board |
| 222869 | 5/1 Secondary reference U.S. Government activity |
NSN 6550-01-607-9206 is a Test Kit,human Chorionic Gonadot, manufactured by Quidel Corp, classified under FSC 6550, In Vitro Diagnostic Substances, Reagents, Test Kits and Sets. Status: active.
NSN 6550-01-607-9206 has 1 manufacturer part number on file: 20110 (Quidel Corp).
Key specifications for 20110: Special Features: FOR THE QUALITATIVE DETECTION OF HUMAN CHORIONIC GONADOTROPIN (HCG) IN SERUM OR URINE FOR THE EARLY DETECTION OF PREGNANCY; 25 MIU/ML SENSITIVITY; INCLUDES TEST CASSETTES, PIPETTES, PACKAGE INSERT, AND PROCEDURE CARD; 50 TESTS; Test Media: SERUM OR URINE; Test Capability Quantity: 50; Part Name Assigned by Controlling Agency: TEST HCG DET PREGANACY TEST URINE SERUM COMBO 50S. 4 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.