Primary Device ID | 00887661613370 |
NIH Device Record Key | 37e12d9c-ff90-4518-92e6-b159861689fb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ASSORTED BRANDS |
Version Model Number | DL4692/12.FTG |
Company DUNS | 062312087 |
Company Name | FGX INTERNATIONAL 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 |