| Primary Device ID | 04056869951386 |
| NIH Device Record Key | 729a96df-ab0c-43d6-923e-25042cbc2d65 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MULTIX Impact E |
| Version Model Number | 11333999 |
| Company DUNS | 654129626 |
| Company Name | Siemens Shanghai Medical Equipment Ltd. |
| 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 | 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 | 04056869951386 [Primary] |
| KPR | System, x-ray, stationary |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-10-04 |
| Device Publish Date | 2022-09-26 |
| 04056869267180 - CIOS SELECT | 2023-06-16 |
| 04056869267197 - CIOS SELECT | 2023-06-15 mobile C-arm; software version VA21 |
| 04056869951386 - MULTIX Impact E | 2022-10-04 |
| 04056869951386 - MULTIX Impact E | 2022-10-04 |
| 04056869279985 - MULTIX Impact | 2021-11-18 |
| 04056869262147 - MULTIX Impact C | 2021-03-30 |
| 04056869239736 - SOMATOM go.Sim | 2020-10-05 |
| 04056869226545 - MULTIX Impact | 2020-10-01 |
| 04056869239743 - SOMATOM go.Open Pro | 2020-09-07 |