Primary Device ID | 04582667985679 |
NIH Device Record Key | 483b045a-79cd-42c4-b509-41bf33dcd5ec |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EYEVAN7285 |
Version Model Number | 170 49 900-G DK.BLU |
Company DUNS | 705184505 |
Company Name | EYEVAN INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
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 | false |