| Primary Device ID | 00653405015102 |
| NIH Device Record Key | f732fb14-6a57-41de-ae61-4b9bf40d1781 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 9037850 |
| Catalog Number | 9037850 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 400 |
| 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 | 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00653405015102 [Unit of Use] |
| GS1 | 20653405015106 [Primary] |
| BYY | TUBE, ASPIRATING, FLEXIBLE, CONNECTING |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-06-14 |
| Device Publish Date | 2022-06-06 |
| 10653405986362 - CONMED | 2026-01-26 Universal Modular Base Cart |
| 30653405986373 - CONMED | 2026-01-26 Universal Modular Cart, Cord Wraps |
| 20653405990182 - CONMED | 2026-01-26 Universal Cart Strap |
| 10653405990734 - Hall® Titan™ | 2026-01-06 Hall® Titan™ XE Single Trigger Battery Handpiece |
| 10653405990741 - Hall® Titan™ | 2026-01-06 Hall® Titan™ XE Dual Trigger Battery Handpiece |
| 30653405990714 - Infinity | 2025-12-09 Infinity Retro-Reamer, 10.5 mm |
| 30653405990707 - BioBrace | 2025-11-25 BioBrace Extra-Articular Ligament Augmentation Kit |
| 00810021867373 - CoLink® | 2025-07-11 CoLink® Afx, Locking Screw, 2.7X14.0MM, 2-Pack |