| Primary Device ID | 00092237626573 |
| NIH Device Record Key | e2c71941-15b3-4b4f-b901-8b44b835a2e6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Richmar EMG Software |
| Version Model Number | EMG-SW |
| Company DUNS | 827221698 |
| Company Name | COMPASS HEALTH BRANDS CORP. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | 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 | 00092237626573 [Primary] |
| HCC | Device, Biofeedback |
| 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 |
| 00092237626887 - TheraTouch SW1 | 2025-04-14 SW1 WIRED HANDPIECE |
| 00092237626955 - TheraTouch SW1 | 2025-04-14 Shockwave CR 15mm Applicator |
| 00092237626962 - TheraTouch SW1 | 2025-04-14 Shockwave CR 20mm Applicator |
| 00092237626764 - TheraTouch SW1 | 2025-04-04 TheraTouch SW1 Portable Shockwave |
| 00092237624166 - Probasics | 2025-03-06 K2 Wheelchair 16x16 w/o Front Riggins |
| 00092237624173 - Probasics | 2025-03-06 K2 Wheelchair 18x16 w/o Front Riggins |
| 00092237624180 - Probasics | 2025-03-06 K2 Wheelchair 20x16 w/o Front Riggins |
| 00815067044108 - MERIDIAN MEDICAL | 2025-03-03 SATINAIR APM-8"W/ANALOG PUMP, 8" AIR - 350 LB CAP (SYSTEM) |