| Primary Device ID | 00810050861984 |
| NIH Device Record Key | f4981ec3-d095-464c-8c6a-3abc2c8f8561 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IV Pole |
| Version Model Number | ST2-541-01 |
| Company DUNS | 556196210 |
| Company Name | LIFEPORT, LLC |
| Device Count | 1 |
| 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 | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810050861984 [Primary] |
| FOX | Stand, Infusion |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-05-11 |
| Device Publish Date | 2022-05-03 |
| 00810050861984 | ASSEMBLY, IV POLE, 16G |
| 00810050862998 | ASSEMBLY, IV POLE, 16G |