| Primary Device ID | 00092237626054 |
| NIH Device Record Key | 548fd7ad-7d46-4249-836d-3bff66060e77 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Richmar EMG Pro |
| Version Model Number | EMG-RP |
| 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 | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| 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 | 00092237626054 [Primary] |
| IPF | Stimulator, Muscle, Powered |
| KPI | Stimulator, Electrical, Non-Implantable, For Incontinence |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-07-08 |
| Device Publish Date | 2024-06-28 |
| 00092237624456 | Richmar EMG Pro |
| 00092237626054 | Richmar EMG Pro Rectal Probe |
| 00092237626047 | Richmar EMG Pro Vaginal Probe |