gudid
Primary ID: P10105-413
iBEAM (UDI P10105-413)
Manufactured by 3C-Medical Intelligence GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for iBEAM - Primary ID P10105-413
Device Regulatory Overview
The iBEAM (Model/Catalog Number: P10105-413) is a medical device manufactured by 3C-Medical Intelligence GmbH. This product is indexed under FDA Product Code / Category Classification IXQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P10105-413
- Product Code / EMDN
- IXQ
- Device Name
- The iBEAM evo Extension H&N is designed to support the patients 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.
- Database Sync Date
- 2026-08-09 09:26:08
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of iBEAM?
The registered manufacturer of record for iBEAM is 3C-Medical Intelligence GmbH.
What is the Primary UDI-DI identifier for iBEAM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P10105-413.
What classification code is assigned to this device?
This device is registered under product classification code IXQ.
Similar Classification Devices (IXQ)
Other Devices by 3C-Medical Intelligence GmbH
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