| Primary Device ID | 00780707000007 |
| NIH Device Record Key | 49031dcc-07d0-4b6e-ac72-8864a9b43b0c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Hydravue |
| Version Model Number | 1 |
| Company DUNS | 840130579 |
| Company Name | United Exchange 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 | 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 | 00780707000007 [Primary] |
| LPN | Accessories, Soft Lens Products |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-06-02 |
| Device Publish Date | 2025-05-23 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() HYDRAVUE 85110459 not registered Dead/Abandoned |
Unilens Corp. 2010-08-18 |