| Primary Device ID | 50023601210000 |
| NIH Device Record Key | a0a8a9c9-1ac2-4d74-bfc9-539eaabd3e1b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | N/A |
| Version Model Number | ACRL-1000 |
| 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 | 00023601210005 [Primary] |
| GS1 | 30023601210006 [Package] Contains: 00023601210005 Package: PK [6 Units] In Commercial Distribution |
| GS1 | 50023601210000 [Package] Contains: 30023601210006 Package: CA [4 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 | 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) |