| Primary Device ID | 50023601220016 | 
| NIH Device Record Key | 63f8b1d9-7410-4bb8-ba1d-73f767dcef54 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | AccuRelief | 
| Version Model Number | ACRL-2001 | 
| 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 | 00023601220011 [Primary] | 
| GS1 | 30023601220012 [Package] Contains: 00023601220011 Package: PK [6 Units] In Commercial Distribution  | 
| GS1 | 50023601220016 [Package] Contains: 30023601220012 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  |