| Primary Device ID | 10845854016442 |
| NIH Device Record Key | fa603539-f42a-4762-9f7f-196f299a2728 |
| Commercial Distribution Discontinuation | 2022-06-06 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | 8973S |
| Catalog Number | 8973S |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 |
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