| Primary Device ID | 00023601200013 | 
| NIH Device Record Key | a387c6de-f8f7-4187-8259-324764bf6552 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | AccuRelief | 
| Version Model Number | ACRL-0001 | 
| Company DUNS | 082522269 | 
| Company Name | Carex Health Brands | 
| Device Count | 4 | 
| 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 | false | 
| Manufacturing Date | false | 
| Expiration Date | true | 
| 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 | 00023601200013 [Primary] | 
| GS1 | 01023601200017 [Unit of Use] | 
| GS1 | 30023601200014 [Package] Package: PK [6 Units] In Commercial Distribution  | 
| GS1 | 50023601200018 [Package] Contains: 30023601200014 Package: CA [8 Units] In Commercial Distribution  | 
| GXY | Electrode, Cutaneous | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2021-02-19 | 
| Device Publish Date | 2016-10-05 | 
| 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  |