| 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 |