| Primary Device ID | 80092237618550 |
| NIH Device Record Key | 69d5e1df-da23-42c9-9776-78e54bed1ae7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | World Wide Medical |
| Version Model Number | DI3302-WWM |
| Company DUNS | 827221698 |
| Company Name | COMPASS HEALTH BRANDS CORP. |
| 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 | true |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 | 00092237618554 [Primary] |
| GS1 | 80092237618550 [Package] Contains: 00092237618554 Package: CA [32 Units] In Commercial Distribution |
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-10-23 |
| Device Publish Date | 2016-10-12 |
| 80092237618604 | ProTENS DUAL COMBO |
| 80092237618581 | ProTENS DUAL STIM |
| 80092237618550 | ProTENS CROSSOVER |
| 80092237618512 | ProTENS One Touch Select |
| 01092237605584 | WWM, K120 Electrode Poly Bag 2 |