Primary Device ID | 04056869050713 |
NIH Device Record Key | 61cad69a-2824-4a5d-943d-8d92a2bb30fd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Multix Fusion Max |
Version Model Number | 11020660 |
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 | 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 | 04056869050713 [Primary] |
KPR | System, x-ray, stationary |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-03-31 |
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 |
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 |