AHLEM
GUDID 03701558412143
Ahlem Eyewear, LLC
Spectacle frame| Primary Device ID | 03701558412143 |
| NIH Device Record Key | 239a9963-a69b-4a79-9670-fb446f3fd216 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AHLEM |
| Version Model Number | OA077-DSTL |
| Company DUNS | 003946572 |
| Company Name | Ahlem Eyewear, LLC |
| 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 | 03701558412143 [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 | 2024-02-07 |
| Device Publish Date | 2024-01-30 |
On-Brand Devices [AHLEM]
Trademark Results [AHLEM]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 AHLEM 88978744 not registered Live/Pending |
Ahlem Eyewear, LLC 2019-09-25 |
 AHLEM 88631233 not registered Live/Pending |
Ahlem Eyewear, LLC 2019-09-25 |
 AHLEM 86331610 4763320 Live/Registered |
Ahlem Eyewear, LLC 2014-07-08 |
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