Primary Device ID | 00842894151938 |
NIH Device Record Key | c83e7038-e2b2-4594-9a0a-f1a761594190 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Clear Readers |
Version Model Number | 1116-200 |
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 | 00842894151938 [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 |