| Primary Device ID | 04719878879958 |
| NIH Device Record Key | 89b6deba-b97b-4712-9ddb-9937b3a4a35e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EBM |
| Version Model Number | EBM VS 1000 |
| Company DUNS | 657261272 |
| Company Name | EBM TECHNOLOGIES INCORPORATED |
| 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 | false |
| 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 |
|---|---|
| GS1 | 04719878879958 [Primary] |
| OUG | Medical Device Data System |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-06-19 |
| Device Publish Date | 2023-06-09 |
| 04719878879996 | UniWeb 360 |
| 04719878879989 | MobiPACS" App 1.2.1, Rad@ |
| 04719878879972 | SoliPACS™ Web Viewer ,version 8.0 |
| 04719878879965 | MobiPACS™ App |
| 04719878879958 | EBM VS 1000 |
| 04719878879941 | SoliPACS™ Client Viewer with SoliPACS™ Gateway |
| 04719878879934 | SoliPACS™ Client Viewer, version 4.0 |
| 04719878879927 | SoliPACS™ Web Viewer ,version 5.0 |
| 04719878879910 | SoliPACS™ Server |