eudamed_udi
Primary ID: 04041314031201
Greifhilfe RFM Basic, kurz (UDI 04041314031201)
Manufactured by Rehaforum Medical GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Greifhilfe RFM Basic, kurz - Primary ID 04041314031201
Device Regulatory Overview
The Greifhilfe RFM Basic, kurz (Model/Catalog Number: 09483514) is a medical device manufactured by Rehaforum Medical GmbH. This product is indexed under FDA Product Code / Category Classification Y242103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 09483514
- Product Code / EMDN
- Y242103
- Device Name
- Greifhilfe RFM Basic, kurz
- Database Sync Date
- 2026-08-09 18:17:38
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 Greifhilfe RFM Basic, kurz?
The registered manufacturer of record for Greifhilfe RFM Basic, kurz is Rehaforum Medical GmbH.
What is the Primary UDI-DI identifier for Greifhilfe RFM Basic, kurz?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04041314031201.
What classification code is assigned to this device?
This device is registered under product classification code Y242103.
Similar Classification Devices (Y242103)
Other Devices by Rehaforum Medical GmbH
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