| Primary Device ID | 50023601290019 |
| NIH Device Record Key | 2966578a-7b9e-4c54-a1e4-fa26bb4e686d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AccuRelief |
| Version Model Number | ACRL-9001 |
| Company DUNS | 082522269 |
| Company Name | Carex Health Brands |
| 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 | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00023601290014 [Primary] |
| GS1 | 30023601290015 [Package] Contains: 00023601290014 Package: PK [6 Units] In Commercial Distribution |
| GS1 | 50023601290019 [Package] Contains: 30023601290015 Package: CA [6 Units] In Commercial Distribution |
| NUH | Stimulator, Nerve, Transcutaneous, Over-The-Counter |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-10-23 |
| Device Publish Date | 2017-04-21 |
| 50023601290019 | AccuRelief Wireless Pain Relief Device |
| 50023601220016 | AccuRelief Single Channel Pain Relief Device |
| 00023601200013 | AccuRelief Universal Supply KIT |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ACCURELIEF 86975656 4630018 Live/Registered |
COMPASS HEALTH BRANDS CORP. 2013-08-19 |
![]() ACCURELIEF 86041329 not registered Dead/Abandoned |
Roscoe Medical, Inc. 2013-08-19 |