| Primary Device ID | 00842894140437 | 
| NIH Device Record Key | c4a5d67f-76bd-48af-a9b2-6a2db504821b | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Clear Readers | 
| Version Model Number | 1102-350 | 
| Company DUNS | 604170506 | 
| Company Name | Diversified Products, 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 | true | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00842894140437 [Primary] | 
| HOI | Spectacle, Magnifying | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2022-11-28 | 
| Device Publish Date | 2022-11-20 | 
Mark Image Registration | Serial  | Company  Trademark Application Date  | 
|---|---|
![]() CLEAR READERS  85826420  4499328 Live/Registered  | 
        Diversified Products, Inc.  2013-01-18  |