| Primary Device ID | 00855859003142 |
| NIH Device Record Key | eebf3c95-743f-4ee9-8075-45d10b54995c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Via |
| Version Model Number | Via 30 mL |
| Company DUNS | 045668792 |
| Company Name | Solv Wellness, LLC |
| 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 | true |
| 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 |
| Phone | 8774217160 |
| help@solvwellness.com | |
| Phone | 8774217160 |
| help@solvwellness.com | |
| Phone | 8774217160 |
| help@solvwellness.com | |
| Phone | 8774217160 |
| help@solvwellness.com | |
| Phone | 8774217160 |
| help@solvwellness.com | |
| Phone | 8774217160 |
| help@solvwellness.com | |
| Phone | 8774217160 |
| help@solvwellness.com | |
| Phone | 8774217160 |
| help@solvwellness.com | |
| Phone | 8774217160 |
| help@solvwellness.com | |
| Phone | 8774217160 |
| help@solvwellness.com | |
| Phone | 8774217160 |
| help@solvwellness.com | |
| Phone | 8774217160 |
| help@solvwellness.com | |
| Phone | 8774217160 |
| help@solvwellness.com | |
| Phone | 8774217160 |
| help@solvwellness.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00855859003142 [Primary] |
| NUC | Lubricant, Personal |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-08-08 |
| Device Publish Date | 2025-07-31 |
| 00855859003111 | Via 3 mL Sample |
| 00855859003081 | Via 30 mL |
| 00855859003142 | Via 30 mL |