Primary Device ID | M722C18334L180560 |
NIH Device Record Key | 772761c8-c140-40b9-ba99-32d7de04d0cc |
Commercial Distribution Discontinuation | 2019-04-11 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | ClearRead +Confirm |
Version Model Number | 2.2.1 |
Company DUNS | 172223922 |
Company Name | Riverain Technologies, 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 | true |
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 Issuing Agency | Device ID |
---|---|
HIBCC | M722C18334L180560 [Primary] |
LLZ | System, Image Processing, Radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-04-12 |
Device Publish Date | 2018-12-13 |
M722C18334L180560 | ClearRead +Confirm on Connect Platform |
M722C19091L190710 | ClearRead +Confirm on Connect Platform |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CLEARREAD +CONFIRM 85539597 4515159 Live/Registered |
RIVERAIN TECHNOLOGIES, LLC 2012-02-10 |