gudid
Primary ID: 4.1
iPlan RT Image (UDI 4.1)
Manufactured by Brainlab SE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for iPlan RT Image - Primary ID 4.1
Device Regulatory Overview
The iPlan RT Image (Model/Catalog Number: 4.1) is a medical device manufactured by Brainlab SE. This product is indexed under FDA Product Code / Category Classification LHN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4.1
- Product Code / EMDN
- LHN
- Device Name
- 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 iPlan RT Image?
The registered manufacturer of record for iPlan RT Image is Brainlab SE.
What is the Primary UDI-DI identifier for iPlan RT Image?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 4.1.
What classification code is assigned to this device?
This device is registered under product classification code LHN.
Similar Classification Devices (LHN)
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