Primary Device ID | M722XD20104T20370 |
NIH Device Record Key | 1d397dc2-deb9-4d30-9b43-6d12c829d389 |
Commercial Distribution Discontinuation | 2020-12-30 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | ClearRead Compare Docker |
Version Model Number | 3.3.1 |
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 | M722XD20104T20370 [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 |
M722XD20239T200370 | ClearRead Compare on Docker Platform |
M722XD20104T20370 | ClearRead Compare on Docker Platform. Primary DI Number should be M722XD20104T200370. Re-entered |
M722XD20104T200370 | ClearRead Compare on Docker Platform. Primary DI Number mistyped as M722XD20104T20370. Originall |
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