| Primary Device ID | 30351688435976 |
| NIH Device Record Key | 1e1e6a20-db66-4656-84bc-e79229a31b2d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Portex |
| Version Model Number | C45031551D-NL |
| 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 | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |