| Primary Device ID | 80092237900433 |
| NIH Device Record Key | 8b665168-3c73-46d3-90b3-e96f3aa86f9a |
| Commercial Distribution Discontinuation | 2019-09-26 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Equipos Private Labeled SuperStim 3" Round |
| Version Model Number | 400-888-EQUIPOS |
| Company DUNS | 080930531 |
| Company Name | Compass Richmar, LLC |
| Device Count | 2 |
| 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 | 00092237900437 [Primary] |
| GS1 | 01092237900436 [Unit of Use] |
| GS1 | 30092237900438 [Package] Contains: 00092237900437 Package: Inner Carton [10 Units] Discontinued: 2019-09-26 Not in Commercial Distribution |
| GS1 | 80092237900433 [Package] Contains: 30092237900438 Package: Master Carton [50 Units] Discontinued: 2019-09-26 Not in Commercial Distribution |
| 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 | 2019-09-27 |
| Device Publish Date | 2018-09-27 |
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