| Primary Device ID | 00850958007374 |
| NIH Device Record Key | c4f4c07b-641e-4719-af70-b1e7608fba3a |
| Commercial Distribution Discontinuation | 2016-08-03 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | ProMed Electrotherapy Electrodes |
| Version Model Number | 203-831 |
| 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 | 00850958007374 [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 | 2016-08-02 |
| 00850958007381 | 2"x 3.5" Cloth |
| 00850958007374 | 3" Round Cloth |
| 00850958007367 | 2" Round Cloth |
| 00850958007350 | 2"x 2" Cloth |
| 00850689007681 | 2"x 3.5" Cloth |
| 00850689007674 | 3" Round Cloth |
| 00850689007667 | 2" Round Cloth |
| 00850689007650 | 2"x 2" Cloth |
| 10850689007688 | 2"x 3.5" Cloth, Case of 10 |
| 10850689007671 | 3" Round Cloth, Case of 10 |
| 10850689007664 | 2" Round Cloth, Case of 10 |
| 10850689007657 | 2"x 2" Cloth, Case of 10 |