| Primary Device ID | 00192896052734 |
| NIH Device Record Key | 32ea3e0b-d275-4bdc-a92b-cc81d743c7bb |
| Commercial Distribution Discontinuation | 2019-03-22 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | MARQUIS PROBE/EXPLORER |
| Version Model Number | 1103-319 |
| Catalog Number | 1103-319 |
| Company DUNS | 040729840 |
| Company Name | SONTEC INSTRUMENTS, INC. |
| 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 |