| Primary Device ID | B504TC0124210 |
| NIH Device Record Key | 52f1c7d8-83f1-4b0c-9dc2-7812b2648689 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Smith and Nephew |
| Version Model Number | 012421 |
| Company DUNS | 016889401 |
| Company Name | Provision |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| 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 |