Cios Fusion
GUDID 04056869009056
mobile C-arm
Siemens Healthcare GmbH
Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital Portable general-purpose fluoroscopic x-ray system, digital| Primary Device ID | 04056869009056 |
| NIH Device Record Key | 81ce14a3-4262-4a65-962d-845312b0c95e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cios Fusion |
| Version Model Number | 10308192 |
| 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 |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04056869009056 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K153244
FDA Product Code
| OXO | Image-intensified fluoroscopic x-ray system, mobile |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
Devices Manufactured by Siemens Healthcare GmbH
| 04056869996172 - AI-Rad Companion (Pulmonary) | 2024-04-15 |
| 04056869964331 - AI-Rad Companion (Pulmonary) | 2024-04-09 |
| 04056869961491 - MAGNETOM Terra.X | 2024-04-03 |
| 04056869973135 - MAGNETOM Terra.X Upgrade | 2024-04-03 |
| 04056869975238 - MAGNETOM Cima.X Fit | 2024-03-13 |
| 04056869991269 - syngo Virtual Cockpit | 2024-01-24 |
| 04056869985947 - Syngo Carbon Clinicals | 2024-01-11 |
| 04056869964546 - syngo Application Software | 2024-01-09 syngo Application Software VE3 |
Trademark Results [Cios Fusion]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CIOS FUSION 79151796 4710153 Live/Registered |
Siemens Healthcare GmbH 2014-07-30 |
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