| Primary Device ID | 00382903033270 |
| NIH Device Record Key | de8817e0-e08b-437b-9ddd-9dbcd56758bc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SafetyGlide Syringe |
| Version Model Number | 303327 |
| Catalog Number | 303327 |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00382903033270 [Primary] |
| FMI | Needle, hypodermic, single lumen |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-09-11 |
| Device Publish Date | 2023-09-01 |
| 00382904449575 - BDXpert™ System | 2025-03-28 BDXpert™ System |
| 00382904490829 - NMIC-312 | 2025-03-28 NMIC-312 |
| 00382904490836 - NMIC/ID-313 | 2025-03-28 NMIC/ID-313 |
| 00382906666482 - N/A | 2025-03-27 BD® CD26 (M-A261) APC |
| 50382903041423 - N/A | 2025-03-25 NEEDLE 23GA 1-1/2IN BNS TW |
| 30382903884378 - BD Insyte Vialon-E 20GA | 2025-03-25 INSYTE VIALON-E 20GA X 1.88IN |
| 00382902411154 - BD Francisella tularensis Antigen | 2025-03-11 Vial Francisella Tularensis Antigen 5 Ml |
| 00382902411161 - BD Francisella tularensis Antisera | 2025-03-11 Vial F Tularensis Antiserum |