gudid
Primary ID: 01543030
FDM-3 System (UDI 01543030)
Manufactured by zebris MEDICAL GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FDM-3 System - Primary ID 01543030
Device Regulatory Overview
The FDM-3 System (Model/Catalog Number: 01543030) is a medical device manufactured by zebris MEDICAL GmbH. This product is indexed under FDA Product Code / Category Classification KHX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 01543030
- Product Code / EMDN
- KHX
- Device Name
- Platform system for pressure distribution measurement under the human feet, intended for the analysis of the static and dynamic loads, as well as the individual gait parameters.
- Database Sync Date
- 2026-08-09 09:06:21
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 FDM-3 System?
The registered manufacturer of record for FDM-3 System is zebris MEDICAL GmbH.
What is the Primary UDI-DI identifier for FDM-3 System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 01543030.
What classification code is assigned to this device?
This device is registered under product classification code KHX.
Similar Classification Devices (KHX)
Other Devices by zebris MEDICAL GmbH
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