Primary Device ID | 00860006442699 |
NIH Device Record Key | 0cdc9102-1129-481b-a2d2-584b8c8558b5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | cmAngio |
Version Model Number | V1.6 |
Company DUNS | 080081187 |
Company Name | Curemetrix, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00860006442699 [Primary] |
QIH | Automated Radiological Image Processing Software |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-05-12 |
Device Publish Date | 2025-05-02 |
00860006442682 | cmAngio is intended to process screening mammograms to aid a qualified interpreting physician in |
00860006442699 | cmAngio is intended to process screening mammograms to aid a qualified interpreting physician in |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() CMANGIO 88840416 not registered Live/Pending |
CureMetrix, Inc. 2020-03-19 |