| Primary Device ID | 20653405012488 |
| NIH Device Record Key | 6650adf2-ec22-4e43-938a-a06123470eb7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 1000 SES |
| Version Model Number | 60-6810-001 |
| Catalog Number | 60-6810-001 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 5 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00653405012484 [Unit of Use] |
| GS1 | 20653405012488 [Package] Contains: 30653405012485 Package: BOX [5 Units] In Commercial Distribution |
| GS1 | 30653405012485 [Primary] |
| FYD | APPARATUS, EXHAUST, SURGICAL |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-10-21 |
| Device Publish Date | 2016-09-24 |
| 40653405032336 | 1000 SES SMOKE EVACUATION SYSTEM, REDUCER |
| 20653405032325 | 1000 SES SMOKE EVACUATION SYSTEM, REDUCER |
| 20653405012570 | 1000 SES SMOKE EVACUATION SYSTEM, FILTER |
| 20653405012495 | 1000 SES SMOKE EVACUATION SYSTEM, LEEP TUBING SET |
| 20653405012488 | 1000 SES SMOKE EVACUATION SYSTEM, LAPARSCOPIC TUBING SET |
| 20653405012471 | 1000 SES SMOKE EVACUATION SYSTEM, HAND HELD TUBING SET |