| Primary Device ID | 04056869964546 |
| NIH Device Record Key | 8b5079b3-a720-49f9-9193-186ce2186a6d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | syngo Application Software |
| Version Model Number | 30000266 |
| 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 | 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 | 04056869964546 [Primary] |
| LLZ | System, image processing, radiological |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-01-09 |
| Device Publish Date | 2024-01-01 |
| 04056869050874 | syngo Application Software VD2 |
| 04056869012902 | syngo Application Software VD1 |
| 04056869124162 | syngo Application Software VE2 |
| 04056869262567 | syngo Application Software VD3; covered by NFJ to K170747/K173611 syngo Application Software VD2 |
| 04056869964546 | syngo Application Software VE3 |
| 04056869964539 | syngo Application Software VE4 |