| Primary Device ID | 80092237900464 |
| NIH Device Record Key | b76d5048-f2f6-4580-8625-5ada0ae0c2a4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Medical Science Products Private Label |
| Version Model Number | 203-482 |
| Company DUNS | 080930531 |
| Company Name | Compass Richmar, LLC |
| Device Count | 4 |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00092237900468 [Primary] |
| GS1 | 01092237900467 [Unit of Use] |
| GS1 | 30092237900469 [Package] Contains: 00092237900468 Package: Inner Carton [10 Units] In Commercial Distribution |
| GS1 | 80092237900464 [Package] Contains: 30092237900469 Package: Master Carton [50 Units] In Commercial Distribution |
| GXY | Electrode, Cutaneous |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2019-01-07 |
| 80092237900471 | 2"x3.5" Foam |
| 80092237900464 | 1.25" Round Foam |