Primary Device ID | 04582669019297 |
NIH Device Record Key | 583661fb-1ce2-45c7-957b-0f646b90694c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EYEVAN7285 |
Version Model Number | 199 46 800-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 |