Prelude (UDI V1. EBRT)
Manufactured by MedCom Gesellschaft fr medizinische Bildverarbeitung mbH
Device Regulatory Overview
The Prelude (Model/Catalog Number: V1. EBRT) is a medical device manufactured by MedCom Gesellschaft fr medizinische Bildverarbeitung mbH. This product is indexed under FDA Product Code / Category Classification LHO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- V1. EBRT
- Product Code / EMDN
- LHO
- Device Name
- The Prelude software supports radiation therapy workflows for IntraOp Mobetron, a radiation treatment device.It assists to find product specific machine parameters for treatment and can send those proposals to the console of the device.The machine parameters are not intended to be used for direct control for the radiation device.
- Database Sync Date
- 2026-08-09 09:53:22
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 Prelude?
The registered manufacturer of record for Prelude is MedCom Gesellschaft fr medizinische Bildverarbeitung mbH.
What is the Primary UDI-DI identifier for Prelude?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is V1. EBRT.
What classification code is assigned to this device?
This device is registered under product classification code LHO.
Similar Classification Devices (LHO)
Other Devices by MedCom Gesellschaft fr medizinische Bildverarbeitung mbH
Programmatic Export
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JSON API Endpoint