| Primary Device ID | 04056869267456 |
| NIH Device Record Key | b6a810fe-4880-4262-a9e5-ef764484b3a7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | syngo.CT Brain Hemorrhage |
| Version Model Number | 11546320 |
| Company DUNS | 313217003 |
| Company Name | Siemens Healthcare GmbH |
| 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 | 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 |
|---|---|
| GS1 | 04056869267456 [Primary] |
| QAS | Radiological computer-assisted triage and notification 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 | 2022-12-08 |
| Device Publish Date | 2022-11-30 |
| 04068151036749 - MAGNETOM Flow.Rise | 2026-01-28 |
| 04056869299556 - MAGNETOM Flow.Neo | 2026-01-27 |
| 04056869299594 - MAGNETOM Flow.Neo | 2026-01-27 |
| 04068151034196 - MAGNETOM Flow.Elite | 2026-01-27 |
| 04068151036732 - MAGNETOM Flow.Elite | 2026-01-27 |
| 04068151047943 - MAGNETOM Flow.Neo | 2026-01-27 |
| 04068151047950 - MAGNETOM Flow.Elite | 2026-01-27 |
| 04056869299297 - MAMMOVISTA B.smart | 2026-01-26 Medical software that provides workflow, reading and reporting support on clinical images |