The Blood Grouping Serum,anti-E, cataloged under National Stock Number 6550-01-345-0670, 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 Ortho Diagnostic Systems Inc. Government technical data includes 5 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. 1 item shares a part number with this NSN in the catalog (possible match — not a government interchangeability claim). Current acquisition status: Active.
| Parameter | Value |
|---|---|
| NSN | 6550-01-345-0670 |
| Primary Part Number | 714630 |
| Item Name | Blood Grouping Serum,anti-E |
| FSC / FSG | 6550 / 65 — In Vitro Diagnostic Substances, Reagents, Test Kits and Sets |
| Manufacturer | Ortho Diagnostic Systems Inc |
| Status | ACTIVE |
| Primary Container Content Quantity | 3.000 MILLILITERS |
| Medical Designation and Grade | UNITED STATES PHARMACOPEIA |
| Primary Container Type | VIAL |
| Physical Form | LIQUID |
| Usage Design | SLIDE AND MODIFIED TUBE TESTS |
| 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 |
|---|---|
| 714630 PRIMARY | Ortho Diagnostic Systems Inc (USA) |
NSN 6550-01-345-0670 is a Blood Grouping Serum,anti-E, manufactured by Ortho Diagnostic Systems Inc, classified under FSC 6550, In Vitro Diagnostic Substances, Reagents, Test Kits and Sets. Status: active.
NSN 6550-01-345-0670 has 1 manufacturer part number on file: 714630 (Ortho Diagnostic Systems Inc).
1 possible match (shared part number, not a government interchangeability claim): 6160-01-426-4245. Verify interchangeability with system specifications before substitution.
Key specifications for 714630: Primary Container Content Quantity: 3.000 MILLILITERS; Medical Designation and Grade: UNITED STATES PHARMACOPEIA; Primary Container Type: VIAL; Physical Form: LIQUID. 5 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.