| Primary Device ID | 00860006442682 |
| NIH Device Record Key | 08658cbe-015a-454f-a9e2-da648444ef64 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | cmAngio |
| Version Model Number | V1.0 |
| 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 | 00860006442682 [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 | 2023-11-08 |
| Device Publish Date | 2023-10-31 |
| 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 |