Clear Readers
GUDID 00037741290094
Diversified Products, Inc.
Magnifying spectacles| Primary Device ID | 00037741290094 |
| NIH Device Record Key | b71378b5-387c-4e2d-836c-03bb5be774a7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Clear Readers |
| Version Model Number | 2900-350 |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00037741290094 [Primary] |
FDA Product Code
| HOI | Spectacle, Magnifying |
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 | 2022-12-08 |
| Device Publish Date | 2022-11-30 |
On-Brand Devices [Clear Readers]
Trademark Results [Clear Readers]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CLEAR READERS 85826420 4499328 Live/Registered |
Diversified Products, Inc. 2013-01-18 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.