eudamed_udi
Primary ID: 04046678010039
Fixi (UDI 04046678010039)
Manufactured by REBOTEC Rehabilitationsmittel GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Fixi - Primary ID 04046678010039
Device Regulatory Overview
The Fixi (Model/Catalog Number: 1860015) is a medical device manufactured by REBOTEC Rehabilitationsmittel GmbH. This product is indexed under FDA Product Code / Category Classification Y120609 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1860015
- Product Code / EMDN
- Y120609
- Device Name
- Rollatoren
- Database Sync Date
- 2026-08-09 16:46:37
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 Fixi?
The registered manufacturer of record for Fixi is REBOTEC Rehabilitationsmittel GmbH.
What is the Primary UDI-DI identifier for Fixi?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04046678010039.
What classification code is assigned to this device?
This device is registered under product classification code Y120609.
Similar Classification Devices (Y120609)
Other Devices by REBOTEC Rehabilitationsmittel GmbH
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