| Primary Device ID | 00888118077004 |
| NIH Device Record Key | a80691d1-014b-4976-a1dc-c3f10c740f8f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LEVEL ONE TRANSBUCCAL |
| Version Model Number | 50-501-29-07 |
| Company DUNS | 826499238 |
| Company Name | KLS-Martin L.P. |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |