| Primary Device ID | 00869202000214 |
| NIH Device Record Key | e5d6b69c-b7ab-4097-ba76-0a9226b5c1e6 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 9.0 |
| Company DUNS | 152007423 |
| Company Name | MEDHOST OF TENNESSEE, INC. |
| 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 | 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 | false |
| OTC Over-The-Counter | false |