MAGNETOM Viato.Mobile 11689652
by Siemens Healthineers EUDAMEDGUDID
Active
Ref 11689652Model MDR_02_IIa_FOR AG S3_ACDV_Magnetom
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number0405686902279W2 | Date10 Jul 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04068151995374 | Date23 Feb 2026 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls on record, checked 24 Oct 2026.
Specification
- Trade Name
- MAGNETOM Viato.Mobile
- Generic Name
- Full-body MRI system, superconducting magnet
- Device Name
- MDR_02_IIa_FOR AG S3_ACDV_Magnetom
- Model / Reference
- 11689652, MDR_02_IIa_FOR AG S3_ACDV_Magnetom
- Primary DI / UDI-DI
- 04068151995374
- Basic UDI-DI
- 0405686902279W2
- 510(k) Number
- FDA Product Code
- MOS, LNI, LNH
- EMDN Code
- Z11050104 Closed magnet MRI scanners with magnetic field less than or equal to 2t
- GMDN Term
- Full-body MRI system, superconducting magnet
- Device Class
- Class IIa EUDAMEDClass II GUDID
- Regulation Number
- 892.1000
- Market of Registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- MRI Safety
- MR Safe
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIa | Class II |
Other devices from Siemens Healthineers
Properties
Other properties (23)
- Sterile: No
- Single Use: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Prescription Use: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Lot / Batch Number: No
- Expiration Date: No
- Manufacturing Date: No