| Primary Device ID | 00860074002245 |
| NIH Device Record Key | 570c0b69-bdda-4198-a2ba-1ceb87f9015c |
| Commercial Distribution Discontinuation | 2023-05-31 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mobius Therapy |
| Version Model Number | PAD2 |
| Company DUNS | 081154948 |
| Company Name | Endless Relief |
| 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 | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| 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 | 00860074002214 [Package] Package: Bag [40 Units] Discontinued: 2023-05-30 In Commercial Distribution |
| GS1 | 00860074002245 [Primary] |
| GS1 | 00860074002252 [Package] Contains: 00860074002214 Package: Case [3 Units] Discontinued: 2023-05-30 In Commercial Distribution |
| GS1 | 00860074002290 [Package] Contains: 00860074002252 Package: Carton [4 Units] Discontinued: 2023-05-30 In Commercial Distribution |
| GXY | Electrode, Cutaneous |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-07-31 |
| Device Publish Date | 2018-06-30 |
| 00860074002245 | PAD2 |
| 00860074002207 | KTR-201 |