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 |