Primary Device ID | 03660576051447 |
NIH Device Record Key | f9979a6e-bd65-484d-975c-b3702a940a0c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Julbo |
Version Model Number | J5464022 |
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 | 03660576051447 [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 |