| Primary Device ID | 50382903861809 |
| NIH Device Record Key | 8380d270-1103-44ad-8a67-55b80eb0cae4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BD IV Start Pak, BD Persist |
| Version Model Number | 386180 |
| Catalog Number | 386180 |
| Company DUNS | 124987988 |
| Company Name | BECTON, DICKINSON AND COMPANY |
| Device Count | 25 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| Device Combination Product | true |
| 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 | 00382903861804 [Unit of Use] |
| GS1 | 30382903861805 [Primary] |
| GS1 | 50382903861809 [Package] Contains: 30382903861805 Package: Case [8 Units] In Commercial Distribution |
| LRS | I.V. start kit |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-12-11 |
| Device Publish Date | 2016-10-03 |
| 50382903861908 | IVSP BL PERSIST OPSITE/TRANSPORE TAPE/GA |
| 50382903861809 | IV START PAK W/PERSIST, OPSITE |
| 50382903861793 | IV START PAK W/PERSIST, TEGADERM, DRAPE |
| 50382903861755 | IVSS RED PERSIST WO TEGADERM MED GLV DRP |
| 50382903861724 | IVSS RED IV ACC WO TEGADERM MED GLVS |
| 50382903861700 | IV START PAK W/PERSIST, TEGADERM |