| Primary Device ID | 30845854040564 |
| NIH Device Record Key | 572ea800-e7b6-4ceb-b664-531424aaf6ca |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | T2530RFB |
| Catalog Number | T2530RFB |
| 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 | false |
| 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 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Angle | 30 degree |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20845854040567 [Primary] |
| GS1 | 30845854040564 [Direct Marking] |
| HRX | ARTHROSCOPE |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
| 10653405008125 - NA | 2024-12-04 CONMED REUSABLE DISPERSIVE ELECTRODE |
| 10653405008132 - NA | 2024-12-04 CONMED REUSABLE PEDIATRIC DISPERSIVE ELECTRODE |
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| 30653405987608 - PlumeSafe® X5™ | 2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit, 220V-240V 50/60 Hz |
| 30653405990141 - PlumeSafe® X5™ | 2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit with PlumeSafe® X5™ Smoke Evacuator Filter, 220V-240V 50/60 Hz |
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| 20653405990137 - BioBrace | 2024-09-30 BioBrace® Reinforced Implant, 35 x 25 mm |