| Primary Device ID | 00092237621967 |
| NIH Device Record Key | e6b146a3-c128-43d5-8312-0ceaab856878 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TwinStim |
| Version Model Number | DS5002-OTC |
| 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 |
| Phone | 800-376-7263 |
| customerservice@compasshealthbrands.com | |
| Phone | 800-376-7263 |
| customerservice@compasshealthbrands.com | |
| Phone | 800-376-7263 |
| customerservice@compasshealthbrands.com | |
| Phone | 800-376-7263 |
| customerservice@compasshealthbrands.com | |
| Phone | 800-376-7263 |
| customerservice@compasshealthbrands.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00092237621967 [Primary] |
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-10-07 |
| Device Publish Date | 2025-09-29 |
| 00092237621974 | Twin Stim OTC Amazon |
| 00092237621967 | TwinStim Plus OTC |