| Primary Device ID | 01023601200029 |
| NIH Device Record Key | d4c08fb8-f083-43d7-a283-dbc081e94205 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | N/A |
| Version Model Number | ACRL-0002 |
| Company DUNS | 082522269 |
| Company Name | Carex Health Brands |
| Device Count | 2 |
| 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 | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00023601200020 [Primary] |
| GS1 | 01023601200029 [Direct Marking] |
| GS1 | 30023601200021 [Package] Contains: 00023601200020 Package: PK [6 Units] In Commercial Distribution |
| GS1 | 50023601200025 [Package] Contains: 30023601200021 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 | 2016-10-12 |
| 50023601290002 | AccuRelief Wireless Remote |
| 30023601255007 | ULTIMATE FOOT CIRCULATOR |
| 00023601255006 | ULTIMATE FOOT CIRCULATOR |
| 50023601230008 | AccuRelief Dual Channel TENS |
| 30023601220005 | AccuRelief Single Channel TENS |
| 50023601210000 | AccuRelief Mini TENS |
| 30023601200229 | MINI TENS SUPPLY KIT 2 PACK of electrodes |
| 50023601200032 | AccuRelief Wireless TENS Supply Kit |
| 01023601200029 | AccuRelief Mini TENS Supply Kit (retail box w/4 bags) |