| Primary Device ID | 40653405081976 |
| NIH Device Record Key | e444663b-8284-450f-bb53-fadb398221de |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | AES-WFC |
| Catalog Number | AES-WFC |
| 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 | false |
| Serial Number | true |
| 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 | 20653405081972 [Primary] |
| GS1 | 30653405081979 [Primary] |
| GS1 | 40653405081976 [Direct Marking] |
| 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 | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-24 |
| 30653405990486 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 6MM X 15MM, TITANIUM |
| 30653405990493 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 6MM X 20MM, TITANIUM |
| 30653405990509 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 7MM X 15MM, TITANIUM |
| 30653405990516 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 7MM X 20MM, TITANIUM |
| 30653405990523 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 7MM X 30MM, TITANIUM |
| 30653405990530 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 8MM X 15MM, TITANIUM |
| 30653405990547 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 8MM X 20MM, TITANIUM |
| 30653405990554 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 8MM X 25MM, TITANIUM |