Identity
- Trade Name
- iBEAM evo Extension H&N EUDAMEDiBEAM FDA UDI
- Generic Name
- Accelerator system table, non-powered FDA UDI
- Device Name
- iBEAM evo Couchtop, iBEAM one Couchtop EUDAMEDThe iBEAM® evo Extension H&N is designed to support the patient’s head and neck region and extends off the end of the iBEAM® evo Couchtop by 400 mm. The small profile (omega shape) optimizes the access to the treatment area, facilitating the use of complex and non coplanar beam angles. FDA UDI
- Model / Reference
- P10105-413 EUDAMEDFDA UDI
- Description
- The iBEAM® evo Extension H&N is designed to support the patient’s head and neck region and extends off the end of the iBEAM® evo Couchtop by 400 mm. The small profile (omega shape) optimizes the access to the treatment area, facilitating the use of complex and non coplanar beam angles. FDA UDI
Identifiers
- Catalog Number
- P10105-413 FDA UDI
- Primary DI / UDI-DI
- 04056719001308 EUDAMEDFDA UDI
- Basic UDI-DI
- 04056719BUDI0000000003HY EUDAMED
- Direct Marketing DI
- 04056719001308 EUDAMED
- FDA Product Code
- IXQ FDA UDI
- EMDN Code
- Z11019080 VARIOUS RADIOTHERAPY AND RADIOSURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Accelerator system table, non-powered FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 892.1980 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
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
No
Serial Number
Yes
Expiration Date
No
Manufacturing Date
Yes
Category: Multi-modality therapeutic radiation phantom, test object
iBEAM evo Extension H&N by 3C-Medical Intelligence GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 04056719BUDI0000000003HY | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- 3C-Medical Intelligence GmbH
- EUDAMED SRN
- DE-MF-000023763
Sources (2)
- EUDAMED aea468c0-439f-48f1-b648-fc2208123b68 61 fields · synced Jun 19, 2026
- FDA UDI dc7c555b-f559-4330-b858-57f6a3fdc713 34 fields · synced May 30, 2026