CIARTIC Move
FDA UDIEUDAMEDClass II (US FDA UDI)
Identity
- Trade Name
- CIARTIC Move EUDAMEDFDA UDI
- Generic Name
- Portable general-purpose fluoroscopic x-ray system, digital FDA UDI
- Device Name
- MDR_01_IIb_FOR_ACDV_CIARTIC Move EUDAMED
- Model / Reference
- 11108130 EUDAMEDFDA UDIMDR_01_IIb_FOR_ACDV_CIARTIC Move EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04056869279619 EUDAMEDFDA UDI
- Basic UDI-DI
- 0405686901983WM EUDAMED
- FDA Product Code
- OWB FDA UDIJAA FDA UDIOXO FDA UDI
- EMDN Code
- Z11039017 MOBILE RADIOSCOPIC UNITS EUDAMED
- GMDN Term
- Portable general-purpose fluoroscopic x-ray system, digital FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 892.1650 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
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
Yes
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
No
Serial Number
Yes
Expiration Date
No
Manufacturing Date
No
Category: Portable general-purpose fluoroscopic x-ray system, digital
CIARTIC Move by Siemens Healthcare — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Siemens Healthcare
Sources (2)
- FDA UDI 58043356-90b5-44d1-8fc2-76c7c32c3dd4 33 fields · synced Sep 17, 2026
- EUDAMED e570e081-43bf-428f-8132-7886e6d93467 61 fields · synced Sep 17, 2026