| Primary Device ID | 50382904001839 |
| NIH Device Record Key | 9e29573e-ed9a-4e42-b68b-e52dab30facf |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BD Syringe NRFit™ Lok |
| Version Model Number | 400183 |
| Catalog Number | 400183 |
| Company DUNS | 001292192 |
| Company Name | BECTON, DICKINSON AND COMPANY |
| Device Count | 1 |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00382904001834 [Primary] |
| GS1 | 30382904001835 [Package] Contains: 00382904001834 Package: Shelfpack [40 Units] In Commercial Distribution |
| GS1 | 50382904001839 [Package] Contains: 00382904001834 Package: Case [4 Units] In Commercial Distribution |
| QEH | Piston Syringe with neuraxial connector – epidural, peripheral, and/or indirect cerebral spinal fluid contact |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-03-29 |
| Device Publish Date | 2022-03-21 |
| 50382904001839 | BD® 50mL Syringe NRFit™ Lok |
| 50382904001822 | BD® 20mL Syringe NRFit™ Lok |
| 30382904001743 | BD® 10mL Syringe NRFit™ Lok |
| 50382904001730 | BD® 5mL Syringe NRFit™ Lok |
| 50382904000504 | BD® 3mL Syringe NRFit™ Lok |