| Primary Device ID | 80092237621475 |
| NIH Device Record Key | 6ee047f4-9fe6-444f-b2a0-889455283639 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Richmar TheraTouch |
| Version Model Number | DQ7200 |
| Company DUNS | 080930531 |
| Company Name | Compass Richmar, LLC |
| 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 | 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 | 00092237621479 [Primary] |
| GS1 | 80092237621475 [Package] Contains: 00092237621479 Package: Master Carton [2 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 | 3 |
| Public Version Date | 2019-10-23 |
| Device Publish Date | 2019-02-08 |
| 80092237621055 | LX2 Laser Light Clinical Device with cluster applicator |
| 80092237621475 | EX4 E-stim Clinical Device (4-channel) |
| 00092237621462 | CX4 Combination E-stim/ Ultrasound Clinical Device (4-channel) |
| 00092237620397 | DX2 Shortwave Diathermy Clinical Device |