gudid
Primary ID: P10105-412
iBEAM (UDI P10105-412)
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 P10105-412
Device Regulatory Overview
The iBEAM (Model/Catalog Number: P10105-412) 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
- P10105-412
- Product Code / EMDN
- IXQ
- Device Name
- The iBEAM evo Extension 415 is designed to support the patients head and neck region and extends off the end of the iBEAM evo Couchtop by 415 mm.
- 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 P10105-412.
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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