| Primary Device ID | 00850689007834 |
| NIH Device Record Key | 4ad7e8f2-3b85-4c00-86ca-93e7a204eef0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Dex Trodes |
| Version Model Number | 202-291 |
| Company DUNS | 080930531 |
| Company Name | Compass Richmar, LLC |
| 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 | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850689007834 [Primary] |
| GXY | Electrode, Cutaneous |
| 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 | 2016-09-01 |
| 00850689007841 | 1.25" Round Foam |
| 00850689007834 | 3"x 5" Foam |
| 00850689007827 | 2" Round Foam |
| 00850689007810 | 2"x 3.5" Foam |
| 00850689007803 | 2"x 3.5" Cloth |
| 00850689007797 | 2" Round Cloth |
| 20850689007791 | 2"x 3.5" Cloth, Case of 10 |
| 10850689007848 | 1.25" Round Foam, Case of 10 |
| 10850689007831 | 3"x 5" Foam, Case of 10 |
| 10850689007824 | 2" Round Foam, Case of 10 |
| 10850689007817 | 2"x 3.5" Foam, Case of 10 |
| 10850689007794 | 2" Round Cloth, Case of 10 |