Primary Device ID | 00812559012010 |
NIH Device Record Key | 90fec805-353c-454a-b29e-8478426d1b43 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NearBright |
Version Model Number | 16239 |
Company DUNS | 126650253 |
Company Name | REICHERT, 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 | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00812559012010 [Primary] |
HOX | Chart, Visual Acuity |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-08-20 |
Device Publish Date | 2025-08-12 |
00812559012010 | 16239 |
00812559012003 | 16238 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() NEARBRIGHT 86680672 4985177 Live/Registered |
Reichert, Inc. 2015-07-01 |