| Primary Device ID | 01092237605584 |
| NIH Device Record Key | 5719e1e7-17fb-4bec-91ef-9cd6957a9d6c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | World Wide Medical |
| Version Model Number | E1P2020WC2WW |
| 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 | 00092237605585 [Primary] |
| GS1 | 01092237605584 [Direct Marking] |
| GS1 | 30092237605586 [Package] Contains: 00092237605585 Package: PK [50 Units] In Commercial Distribution |
| GS1 | 80092237605581 [Package] Contains: 30092237605586 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 |
| 80092237618604 | ProTENS DUAL COMBO |
| 80092237618581 | ProTENS DUAL STIM |
| 80092237618550 | ProTENS CROSSOVER |
| 80092237618512 | ProTENS One Touch Select |
| 01092237605584 | WWM, K120 Electrode Poly Bag 2 |