eudamed_udi
Primary ID: 04041314034905
Actimo Light (UDI 04041314034905)
Manufactured by Rehaforum Medical GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Actimo Light - Primary ID 04041314034905
Device Regulatory Overview
The Actimo Light (Model/Catalog Number: 12727397) 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
- 12727397
- Product Code / EMDN
- Y120606
- Device Name
- Actimo Light
- Database Sync Date
- 2026-08-09 16:46:32
Full Regulatory Attributes
đź”’ Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Actimo Light?
The registered manufacturer of record for Actimo Light is Rehaforum Medical GmbH.
What is the Primary UDI-DI identifier for Actimo Light?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04041314034905.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint