| Primary Device ID | 03660576906587 |
| NIH Device Record Key | aa578ad4-d88d-403e-aa8a-d37d45599836 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Julbo |
| Version Model Number | J0209050 |
| Company DUNS | 149276235 |
| Company Name | Julbo 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 03660576906587 [Primary] |
| HQY | Sunglasses (Non-Prescription Including Photosensitive) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-12-09 |
| Device Publish Date | 2022-12-01 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() JULBO 79113970 4315351 Live/Registered |
JULBO 2012-03-09 |
![]() JULBO 75509920 2334556 Live/Registered |
JULBO 1998-06-29 |