eudamed_udi
Primary ID: 04041314036237
Actimo Arthro (UDI 04041314036237)
Manufactured by Rehaforum Medical GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Actimo Arthro - Primary ID 04041314036237
Device Regulatory Overview
The Actimo Arthro (Model/Catalog Number: 13427929) is a medical device manufactured by Rehaforum Medical GmbH. This product is indexed under FDA Product Code / Category Classification Y120606 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 13427929
- Product Code / EMDN
- Y120606
- Device Name
- Actimo Arthro
- Database Sync Date
- 2026-08-09 19:01:14
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 Actimo Arthro?
The registered manufacturer of record for Actimo Arthro is Rehaforum Medical GmbH.
What is the Primary UDI-DI identifier for Actimo Arthro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04041314036237.
What classification code is assigned to this device?
This device is registered under product classification code Y120606.
Similar Classification Devices (Y120606)
Other Devices by Rehaforum Medical GmbH
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