Primary Device ID | 08717872032085 |
NIH Device Record Key | 206a004d-1423-4c58-a0be-b27af8c09d4e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EVA NEXUS™ Digital Overlay System |
Version Model Number | 9000.DOS01 |
Company DUNS | 407522184 |
Company Name | D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. |
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 | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08717872032085 [Primary] |
HQC | Unit, Phacofragmentation |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-07-11 |
Device Publish Date | 2022-07-01 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EVA NEXUS 79292807 not registered Live/Pending |
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. 2020-07-16 |
EVA NEXUS 79272086 not registered Live/Pending |
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. 2019-07-25 |