eudamed_udi
Primary ID: 04046678004359
Berlin (UDI 04046678004359)
Manufactured by REBOTEC Rehabilitationsmittel GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Berlin - Primary ID 04046678004359
Device Regulatory Overview
The Berlin (Model/Catalog Number: 3440300) 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
- 3440300
- Product Code / EMDN
- Y091203
- Device Name
- Dusch-ToilettenrollstĂĽhle
- Database Sync Date
- 2026-08-09 16:28:46
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 Berlin?
The registered manufacturer of record for Berlin is REBOTEC Rehabilitationsmittel GmbH.
What is the Primary UDI-DI identifier for Berlin?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04046678004359.
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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