| Primary Device ID | 10653405033707 |
| NIH Device Record Key | 94b33dbb-3a1d-4e0c-a9ac-448426c0fe47 |
| Commercial Distribution Discontinuation | 2023-12-01 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | 60-0930-002 |
| Catalog Number | 60-0930-002 |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10653405033707 [Primary] |
| GS1 | 20653405033704 [Primary] |
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2023-12-04 |
| Device Publish Date | 2016-09-24 |
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