gudid
Primary ID: P10105-213
Connexion (UDI P10105-213)
Manufactured by 3C-Medical Intelligence GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Connexion - Primary ID P10105-213
Device Regulatory Overview
The Connexion (Model/Catalog Number: P10105-213) 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
- P10105-213
- Product Code / EMDN
- IXQ
- Device Name
- Providing patient-specific immobilization for head and neck treatments often require a variety of immobilization devices. The Connexion Head and Neck Module provides a dedicated solution to support head and neck immobilization, by providing a common interface to not only Elekta immobilization devices, but also other commonly used third party accessories.
- 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 Connexion?
The registered manufacturer of record for Connexion is 3C-Medical Intelligence GmbH.
What is the Primary UDI-DI identifier for Connexion?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P10105-213.
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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