| Primary Device ID | 10850689007770 |
| NIH Device Record Key | 1adbe011-8df9-4e39-adfc-60ff24a64c33 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Medi-Trode Platinum |
| Version Model Number | 202-093 |
| 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 | 10850689007770 [Primary] |
| GXY | Electrode, Cutaneous |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2021-02-19 |
| Device Publish Date | 2016-11-18 |
| 00850689007780 | 2" x 3.5" Foam |
| 00850689007773 | 2"x 2" Foam |
| 10850689007787 | 2" x 3.5" Foam, Case of 10 |
| 10850689007770 | 2"x 2" Foam, Case of 10 |