| Primary Device ID | 30382902206904 |
| NIH Device Record Key | 5771b8ba-b4ff-43a4-8e27-86b0e5a140c0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BD BBL Polyester Fiber-Tipped Applicator Swab |
| Version Model Number | 220690 |
| Catalog Number | 220690 |
| Company DUNS | 122561087 |
| Company Name | BECTON, DICKINSON AND COMPANY |
| Device Count | 1000 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | 00382902206903 [Unit of Use] |
| GS1 | 30382902206904 [Primary] |
| LIO | Device, specimen collection |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2018-05-25 |
| 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 |