Primary Device ID | 04582669019785 |
NIH Device Record Key | 18d0d0d8-e67f-49d4-937e-9c57c076e580 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EYEVAN7285 |
Version Model Number | 361E 49 359-G DK.BR |
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 |