eudamed_udi
Primary ID: 07613365500073
Ganshorn.LFX (UDI 07613365500073)
Manufactured by Ganshorn Medizin Electronic GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ganshorn.LFX - Primary ID 07613365500073
Device Regulatory Overview
The Ganshorn.LFX (Model/Catalog Number: 015000215) is a medical device manufactured by Ganshorn Medizin Electronic GmbH. This product is indexed under FDA Product Code / Category Classification Z12159092 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 015000215
- Product Code / EMDN
- Z12159092
- Device Name
- Ganshorn.LFX
- Database Sync Date
- 2026-08-09 18:21:12
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 Ganshorn.LFX?
The registered manufacturer of record for Ganshorn.LFX is Ganshorn Medizin Electronic GmbH.
What is the Primary UDI-DI identifier for Ganshorn.LFX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07613365500073.
What classification code is assigned to this device?
This device is registered under product classification code Z12159092.
Similar Classification Devices (Z12159092)
Other Devices by Ganshorn Medizin Electronic GmbH
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