| Primary Device ID | 50382903680400 |
| NIH Device Record Key | 26765fb6-28d0-4853-a992-cac4bc44b669 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BD Vacutainer® Lithium Heparin 4.0 mL |
| Version Model Number | 368040 |
| Catalog Number | 368040 |
| Company DUNS | 001292192 |
| Company Name | BECTON, DICKINSON AND COMPANY |
| Device Count | 1000 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00382903680405 [Unit of Use] |
| GS1 | 50382903680400 [Primary] |
| GIM | Tubes, vacuum sample, with anticoagulant |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-07-28 |
| 00382903024353 - N/A | 2025-08-04 TIP CAP ENTERAL SYRINGES STERILE |
| 00382903052752 - BD Integra | 2025-08-04 NEEDLE INTEGRA 18X1-1/2 BLUNT FILL |
| 00382903064137 - BD PosiFlush | 2025-08-04 SYRINGE 3ML HEPARIN 10 UNIT |
| 00382903064144 - BD PosiFlush | 2025-08-04 SYRINGE 5ML HEPARIN 10 UNIT |
| 00382903064236 - BD PosiFlush | 2025-08-04 SYRINGE 3ML HEPARIN 100 UNIT |
| 00382903064243 - BD PosiFlush | 2025-08-04 SYRINGE 5ML HEPARIN 100 UNIT |
| 00382903065455 - BD PosiFlush | 2025-08-04 SYRINGE 5ML SALINE 5ML FILL |
| 00382903065462 - BD PosiFlush | 2025-08-04 SYRINGE 10ML REG PR SALINE 10ML FILL |