| Primary Device ID | 30351688423867 |
| NIH Device Record Key | da7a0c5d-855d-47bd-901d-74b13fcb412b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Portex |
| Version Model Number | 482804 |
| Company DUNS | 215591523 |
| Company Name | Smiths Medical International Ltd |
| 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 | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | true |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |