eudamed_udi
Primary ID: 04046678009125
Genf (UDI 04046678009125)
Manufactured by REBOTEC Rehabilitationsmittel GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Genf - Primary ID 04046678009125
Device Regulatory Overview
The Genf (Model/Catalog Number: 3465440) is a medical device manufactured by REBOTEC Rehabilitationsmittel GmbH. This product is indexed under FDA Product Code / Category Classification Y091203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3465440
- Product Code / EMDN
- Y091203
- Device Name
- Dusch-ToilettenrollstĂĽhle
- Database Sync Date
- 2026-08-09 16:30:04
Full Regulatory Attributes
đź”’ Token Gated
{
"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 Genf?
The registered manufacturer of record for Genf is REBOTEC Rehabilitationsmittel GmbH.
What is the Primary UDI-DI identifier for Genf?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04046678009125.
What classification code is assigned to this device?
This device is registered under product classification code Y091203.
Similar Classification Devices (Y091203)
Other Devices by REBOTEC Rehabilitationsmittel GmbH
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