| Primary Device ID | 01092237611677 |
| NIH Device Record Key | 818502d6-7e11-491c-9f63-d5cb8985c514 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TENSPros |
| Version Model Number | E1P2020WC2-TP |
| Company DUNS | 827221698 |
| Company Name | COMPASS HEALTH BRANDS CORP. |
| 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 | 00092237611678 [Primary] |
| GS1 | 01092237611677 [Direct Marking] |
| GS1 | 30092237611679 [Package] Contains: 00092237611678 Package: PK [50 Units] In Commercial Distribution |
| GS1 | 80092237611674 [Package] Contains: 30092237611679 Package: CA [8 Units] 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 | 2018-03-29 |
| Device Publish Date | 2016-10-17 |
| 01092237611677 | TENS Pro 2 x2 White Cloth |
| 80092237611667 | TENS Pro Digital TENS/EMS |
| 80092237611650 | TENS Pro Digital TENS |