| Primary Device ID | 10653405008545 |
| NIH Device Record Key | fc6f324d-2157-42e8-a229-63c6caa7e9a0 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 60-0823-001 |
| Catalog Number | 60-0823-001 |
| 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 |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10653405008545 [Direct Marking] |
| GS1 | 20653405008542 [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 | 4 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
| 10653405000020 - NA | 2024-06-06 ECG LEADWIRES |
| 10653405004578 - NA | 2024-06-06 5-LEAD COMBINER |
| 10653405004608 - NA | 2024-06-06 RE-ORDER TAG |
| 10653405004622 - NA | 2024-06-06 ECG CABLES |
| 10653405064220 - NA | 2024-06-06 ECG LEADWIRES |
| 30845854080751 - PENADAPT | 2024-05-03 PenAdapt Electrosurgical Pencil Adapter 1 ft (30.5cm) tubing |
| 30845854061767 - NA | 2024-05-03 EY Tubing Kit 1-3/8 in (35mm) x 6 ft (1.8m) tube and six 2 ft (.6m) tubes with integral wand & sponge guard |
| 30845854045798 - CrossFT | 2024-04-26 CrossFT Knotless Biocomposite 4.0 mm Suture Anchor with one 2 mm Hi-Fi Tape (Blue) |