| Primary Device ID | 80092237618642 |
| NIH Device Record Key | 6ee7f5a0-1d48-47ba-a3d4-186ee2e30c86 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LG Med Supply |
| Version Model Number | DS2219 |
| Company DUNS | 827221698 |
| Company Name | COMPASS HEALTH BRANDS CORP. |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00092237618646 [Primary] |
| GS1 | 80092237618642 [Package] Contains: 00092237618646 Package: CA [32 Units] In Commercial Distribution |
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief |
| 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 |
| 80092237618819 | TENS 7000 (LGMedSupply) |
| 80092237618796 | LG SMART- Digital TENS w/10 |
| 80092237618789 | LG TEC Elite - TENS/EMS |
| 80092237618772 | LG QUAD Combo - |
| 80092237618765 | TENS 3000 (LGMedSupply) |
| 80092237618642 | LG-Tec Combo |
| 80092237618505 | EMS 7500 2nd Gen |
| 80092237613739 | LG TEC Multi - |
| 80092237611568 | LG Pro Series 2nd Edition |
| 00092237600115 | LG 8TM Elite - private Label |
| 80092237605819 | LG 8TM Elite - private Label |