Primary Device ID | M722XD20104L20370 |
NIH Device Record Key | 67783557-25f3-4a72-8e79-8d3c42fa5aa2 |
Commercial Distribution Discontinuation | 2020-12-30 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | ClearRead Confirm Docker |
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 | M722XD20104L20370 [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 | 2020-12-31 |
Device Publish Date | 2020-05-19 |
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M722XD20104L20370 | ClearRead Confirm on Docker Platform Primary DI Number should be M722XD20104L200370. Re-entered |
M722XD20104L200370 | ClearRead Confirm on Docker Platform Originally mistyped as M722XD20104L20370. Originally entere |
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