E5 eyevan
GUDID 04582669031046
EYEVAN INC.
Spectacle frame| Primary Device ID | 04582669031046 |
| NIH Device Record Key | f31a6410-0536-4190-a3a9-74f7ce881ff2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | E5 eyevan |
| Version Model Number | P22E 46 RUWG |
| 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 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04582669031046 [Primary] |
FDA Product Code
| HQZ | Frame, Spectacle |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-07-01 |
| Device Publish Date | 2025-06-23 |
On-Brand Devices [E5 eyevan]
Trademark Results [E5 eyevan]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 E5 EYEVAN 79393008 not registered Live/Pending |
KABUSHIKI KAISHA EYEVAN 2024-02-13 |
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