eudamed_udi
Primary ID: 04041314020533
Duschschemel RFM (UDI 04041314020533)
Manufactured by Rehaforum Medical GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Duschschemel RFM - Primary ID 04041314020533
Device Regulatory Overview
The Duschschemel RFM (Model/Catalog Number: 03567799) is a medical device manufactured by Rehaforum Medical GmbH. This product is indexed under FDA Product Code / Category Classification Y093303 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 03567799
- Product Code / EMDN
- Y093303
- Device Name
- Duschschemel RFM
- Database Sync Date
- 2026-08-09 18:46:38
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 Duschschemel RFM?
The registered manufacturer of record for Duschschemel RFM is Rehaforum Medical GmbH.
What is the Primary UDI-DI identifier for Duschschemel RFM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04041314020533.
What classification code is assigned to this device?
This device is registered under product classification code Y093303.
Similar Classification Devices (Y093303)
Other Devices by Rehaforum Medical GmbH
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